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Mac Laryngoscope Set – Macintosh Curved Blade Laryngoscopy, Sizes 1–4, LED Illumination

SKU: PS-OT-0983
The Mac Laryngoscope Set from Peak Surgicals (SKU: PS-OT-0983) is a four-blade Macintosh curved laryngoscope set with LED illumination, available in Stainless Steel and Fiber Optic configurations, providing the complete...

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$49.50
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Mac Laryngoscope Set – Macintosh Curved Blade Laryngoscopy, Sizes 1–4, LED Illumination
Regular price $49.50
Regular price Sale price $49.50 (-0%)
Material: Stainless Steel
Mac Laryngoscope Set
Mac Laryngoscope Set – Macintosh Curved Blade Laryngoscopy, Sizes 1–4, LED Illumination
$49.50

The Mac Laryngoscope Set from Peak Surgicals (SKU: PS-OT-0983) is a four-blade Macintosh curved laryngoscope set with LED illumination, available in Stainless Steel and Fiber Optic configurations, providing the complete Macintosh blade series — sizes 1, 2, 3, and 4 — on a shared laryngoscope handle for orotracheal intubation across the full adult and paediatric patient size range. The Macintosh blade is the curved laryngoscope blade design originally described by Sir Robert Macintosh in 1943 and used in the majority of routine orotracheal intubations worldwide — the blade is advanced along the right side of the tongue, sweeping the tongue leftward into the flange of the blade, and the tip is placed in the vallecula between the base of the tongue and the epiglottis, where upward traction on the handle at 45 degrees to the horizontal tensions the hyoepiglottic ligament and indirectly elevates the epiglottis to expose the glottis. The Mac Laryngoscope Set is used by anaesthetists, emergency physicians, critical care physicians, and airway management teams in operating theatres, emergency departments, intensive care units, and pre-hospital settings for general anaesthesia induction intubation, rapid sequence intubation, and emergency airway management where Macintosh blade technique is the preferred or primary approach.

Macintosh Curved Blade Technique: Vallecula Placement, Tongue Displacement, and Indirect Epiglottis Elevation

The Macintosh curved blade achieves glottic exposure through a specific mechanism that distinguishes it from straight blade laryngoscopy — the blade tip enters the vallecula rather than contacting the epiglottis directly. The Macintosh blade's curved profile matches the natural curvature of the posterior tongue and oropharynx, allowing it to be advanced smoothly along the midline-right tongue surface to the vallecula without requiring the operator to force the instrument around the natural anatomical curve. The broad flange on the left face of the blade sweeps and holds the tongue leftward and out of the line of sight as the blade advances, creating the visual corridor from the oral commissure to the glottis. When the blade tip reaches the vallecula, upward and forward traction on the handle — strictly along the handle axis, not rotating against the upper teeth as a fulcrum — applies tension to the hyoepiglottic ligament, which runs from the epiglottis to the hyoid bone and base of tongue. This ligament traction draws the epiglottis anteriorly and upward without the blade tip directly lifting it, providing the indirect epiglottis elevation that characterises Macintosh technique. The indirect technique is preferred for routine adult intubation because it leaves more space in the right side of the oral cavity for the endotracheal tube to be passed under direct vision alongside the blade, and because it stimulates the laryngeal surface less than direct epiglottis contact, reducing laryngospasm risk in lighter planes of anaesthesia.

Four Macintosh Blade Sizes: Clinical Selection by Patient Age and Anatomy

Macintosh blade size selection determines both the quality of glottic exposure and the safety of the intubation procedure — a blade that is too short fails to reach the vallecula or produces insufficient epiglottis elevation, and a blade that is too long risks advancing the tip into the oesophageal inlet, risking oesophageal intubation or pharyngeal trauma. Size 1 is the paediatric Macintosh blade for children from approximately 2 to 4 years of age, providing the short length needed for the small oropharyngeal dimension of young children. Size 2 covers the age range from approximately 4 to 12 years and is also used for small adults, adults with a short oral-to-glottis distance, and for procedures where a smaller blade profile is needed without defaulting to the neonatal-infant Miller blade. Size 3 is the standard adult blade used for the large majority of routine adult orotracheal intubations — in adults of normal body habitus it provides the correct combination of blade length to reach the vallecula, flange width to displace the tongue, and blade curvature to match the oropharyngeal axis without excess length. Size 4 is the large adult blade for tall patients, patients with long necks, obese patients with a large tongue and limited mouth opening, and patients with an anterior larynx where the standard size 3 blade does not provide adequate vallecula depth. Having all four sizes on a single shared handle allows the anaesthetist to switch blade size immediately during an intubation attempt if the initial size selection proves inadequate.

Stainless Steel and Fiber Optic Configurations

The Mac Laryngoscope Set is available in Stainless Steel and Fiber Optic configurations with identical blade geometry and handle design, differing only in the light transmission mechanism. The Stainless Steel configuration positions the LED light source at the blade surface — either at the blade tip or the flange — providing direct LED-to-target illumination suitable for routine clinical use in operating theatres and emergency departments. The Fiber Optic configuration transmits LED light from the handle through a glass or polymer optical fibre bundle to the blade tip, delivering the illumination at the point of maximum clinical need — the glottis — rather than from a proximal blade position. Fiber optic tip illumination produces a more uniform and concentrated light spot at the laryngeal inlet, with less light scatter in the pharynx above the blade, which is clinically advantageous in patients with blood, secretions, or vomit in the pharynx that scatter proximal blade light and reduce glottic visibility. In both configurations the LED source eliminates the incandescent bulb failure mode that was the primary in-procedure equipment failure of older laryngoscope designs, ensuring consistent maximum brightness at every intubation attempt regardless of how many previous cases the instrument has been used for. The Stainless Steel blades are fully autoclave compatible; confirm the specific reprocessing method for the Fiber Optic configuration with Peak Surgicals before procurement.

CE Mark, ISO 13485, and FDA Certification

The Mac Laryngoscope Set is manufactured under CE Mark, ISO 13485, and FDA compliant quality standards. ISO 13485 certification confirms Peak Surgicals maintains a documented quality management system covering design control, LED component qualification, blade dimensional consistency, and manufacturing process validation for active diagnostic instruments used in critical airway management. CE Mark confirms conformity with EU MDR requirements for active non-implantable medical devices — laryngoscopes are classified as active devices due to their integral LED electrical light source. FDA compliance supports procurement for US hospitals, anaesthesia departments, emergency medicine units, and critical care facilities requiring verified regulatory documentation. Hospital equipment committees and anaesthesia department procurement officers can request CE, ISO 13485, and FDA documentation from Peak Surgicals to satisfy institutional vendor qualification and medical device regulatory review requirements.

Product Specifications

SKU PS-OT-0983
Product Name Mac Laryngoscope Set
Price $49.50 USD
Material Variants Stainless Steel / Fiber Optic (specify on order)
Blade Type Macintosh curved blade (vallecula placement, indirect epiglottis elevation)
Blade Sizes 1 (small paediatric), 2 (paediatric/small adult), 3 (standard adult), 4 (large adult)
Illumination LED
Instrument Category Anaesthesia / Emergency Medicine — Macintosh Direct Laryngoscopy Set
Procedure Orotracheal intubation, rapid sequence intubation, emergency airway management
Clinical Settings Operating theatre, emergency department, ICU, pre-hospital
Reusable Yes
Sterilization Autoclave compatible (stainless steel); confirm fiber optic reprocessing
Certifications CE Mark, ISO 13485, FDA
Warranty 1 Year
MOQ 1 Set
OEM / Custom Orders Available
After-Sale Service Return and Replacement

Frequently Asked Questions

What is the difference between the Mac Laryngoscope Set and the Mac and Miller Laryngoscope Set also available from Peak Surgicals?
The Mac Laryngoscope Set (PS-OT-0983, $49.50) contains only the four Macintosh curved blade sizes (1, 2, 3, 4) for indirect vallecula-technique intubation. The Mac and Miller Laryngoscope Set (PS-OT-0981, $77.00) contains both the complete Macintosh curved blade series and the complete Miller straight blade series, providing ten blades covering both indirect Macintosh technique and direct Miller technique across the full range from neonates to large adults. The Mac Laryngoscope Set is appropriate for departments that use exclusively Macintosh technique for routine adult and paediatric intubation — the large majority of general anaesthesia and emergency intubations in patients aged 2 years and above. The Mac and Miller set is the choice for departments managing neonates and infants requiring Miller 00 and 0 blades, or for departments that maintain both blade types for operator preference and difficult airway scenarios.

Which Macintosh blade size should be used for a standard adult patient?
Macintosh size 3 is the standard blade for adult intubation in patients of normal body habitus — it is the most widely used laryngoscope blade in anaesthesia and emergency medicine worldwide. The size 3 blade provides the correct combination of length to reach the vallecula in a standard adult oropharyngeal dimension, flange width to displace the tongue, and curvature to match the oropharyngeal axis without excess blade length that would risk advancing into the oesophageal inlet. Size 4 is selected for tall patients, patients with a long neck, obese patients with a large tongue, patients with limited mouth opening requiring a longer blade to reach the vallecula, and patients with an anterior larynx where the standard size 3 does not achieve adequate hyoepiglottic ligament tension at the vallecula depth available. Size 2 is used for children aged approximately 4–12 years and for small adults where the size 3 blade is visibly oversized relative to the oral aperture. The correct size is confirmed by the quality of glottic exposure on the first blade insertion — if the epiglottis is not elevated adequately at the correct handle traction angle, the next size up is the immediate solution.

Why is Macintosh technique preferred over Miller technique for routine adult intubation?
The Macintosh curved blade's indirect epiglottis elevation technique is preferred for routine adult intubation for three clinical reasons. First, the indirect technique leaves substantially more room in the right side of the oral cavity for the endotracheal tube to be passed alongside the blade under direct vision — the Miller blade's straight profile occupies more of the right oral space and the tube must be passed with the blade tip directly lifting the epiglottis, requiring more precise coordination of blade position and tube trajectory. Second, the Macintosh blade's broad tongue-displacing flange creates a larger glottic visual field in most adults than the narrower Miller blade in the same patient — the wide flange moves more tongue bulk out of the visual axis, producing a broader line of sight to the glottis. Third, indirect epiglottis elevation produces less direct stimulation of the laryngeal surface than the Miller blade tip lifting the epiglottis directly, reducing the risk of laryngospasm in patients under lighter anaesthetic depth during rapid sequence intubation. The Miller blade's advantages over the Macintosh — better glottic exposure in neonates, infants, and patients with anterior larynges — become important in specific anatomical situations rather than in the general adult intubation population.

How should the Mac Laryngoscope Set be sterilized between uses?
The Stainless Steel configuration of the Mac Laryngoscope Set is compatible with steam autoclave sterilization, which is the recommended reprocessing method for reusable metal laryngoscope blades in hospital settings per standard infection control guidelines. Before autoclaving, the blade should be separated from the handle, cleaned of all secretions and blood under running water with a brush, inspected for integrity of the LED light source contact and the hinge mechanism, and then processed through the standard autoclave cycle used at the institution for stainless steel surgical instruments. The handle containing the battery and LED electrical components requires specific reprocessing compatible with its electronic components — most laryngoscope handles are wiped clean and disinfected with an approved surface disinfectant rather than autoclaved. For the Fiber Optic configuration, the optimal reprocessing method for the fibre bundle assembly should be confirmed with Peak Surgicals before procurement, as optical fibre components may have specific temperature or chemical exposure limitations that differ from standard stainless steel blade processing.

What certifications does the Mac Laryngoscope Set carry?
The Mac Laryngoscope Set carries CE Mark, ISO 13485, and FDA compliance certification. CE Mark confirms the set meets EU MDR requirements for active non-implantable medical devices — laryngoscopes are active devices because they contain an integral LED light source, requiring conformity assessment under the active device pathway rather than the passive instrument pathway. ISO 13485 certification confirms Peak Surgicals operates a quality management system covering design control, LED source qualification, blade dimensional tolerancing, hinge mechanism reliability, and post-market surveillance specific to active diagnostic instruments. FDA compliance supports procurement for US anaesthesia departments, emergency departments, and critical care units where FDA-compliant documentation is required for active airway management devices. Procurement departments should request the CE Declaration of Conformity and ISO 13485 certification documents from Peak Surgicals when placing orders for institutional equipment inventories requiring formal regulatory documentation.

At Peak Surgicals, customer satisfaction and product quality are important to us. We offer a straightforward 30-day return policy, allowing eligible items to be returned within 30 days of delivery.

Eligibility for Returns

To qualify for a return, the item must be unused, in its original condition, and returned in the original packaging with tags, labels, and proof of purchase included.

Items must not show signs of use, alteration, damage, sterilization, or clinical handling after delivery.

How to Initiate a Return

To start a return, please contact us at info@peaksurgicals.com with your order number, product details, and reason for return.

Approved returns should be sent to:
Peak Surgicals
364 E Main Street
Middletown, DE 19709
Delaware, United States

Return Shipping Costs

No Restocking Fee: We do not charge restocking fees on approved returns.

Free Returns: If the item is incorrect, defective, or damaged during shipping, Peak Surgicals will cover the return shipping cost.

Customer Responsibility: If the customer ordered the wrong item or no longer needs the product, the customer is responsible for the return shipping cost.

Return Conditions

Returned products must be received in new, unused condition with all labels, packaging, and documentation intact. Items that are used, damaged, altered, incomplete, or returned without approval may not be eligible for a refund.

Refund Process

Once your return is received and inspected, we will notify you whether the refund has been approved. Approved refunds will be processed to the original payment method within 10 business days.

Please note that your bank or credit card provider may require additional time to post the refund to your account.

Damaged, Defective, or Incorrect Items

Please inspect your order immediately after delivery. If your item is defective, damaged, or incorrect, contact us at info@peaksurgicals.com as soon as possible with your order number and clear photos of the product and packaging.

Exceptions and Non-Returnable Items

Certain items may not be eligible for return, including customized products, personalized instruments, special-order items, clearance items, sale items, and gift cards.

Exchanges

For exchanges, please return the original item after approval and place a new order for the replacement item. This helps ensure faster processing and accurate product selection.

Worldwide Shipping

Peak Surgicals supplies surgical, dental, orthopedic, gynecology, and veterinary instruments to healthcare professionals, clinics, hospitals, distributors, and procurement buyers worldwide.

European Union Customers

For orders shipped to the European Union, customers may have the right to cancel or return an eligible order within 14 days of receipt, provided the item is unused, in its original condition, and returned with all original packaging and proof of purchase.

Contact Us

For return, refund, or exchange inquiries, please contact us:

Phone: +1 315 526 9968
Email: info@peaksurgicals.com

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