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PEAK SURGICALS

Micro Open Hand Drill with Exposed Gear Drive for Small-Bone Fixation

Micro Open Hand Drill with Exposed Gear Drive for Small-Bone Fixation

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SKU:PS-OP-5828

Regular price $192.12 USD
Regular price Sale price $192.12 USD
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Micro Open Hand Drill, SKU PS-OP-5828 and catalog model PS-320.040, is a compact manually operated orthopedic bone drill manufactured from German stainless steel with an exposed gear-driven mechanism. The instrument transfers rotational input from its hand crank through the visible transmission to the distal spindle, supporting controlled bone-channel preparation without an electric, battery-powered, or pneumatic drive unit. Its micro-pattern configuration is suited to guided drilling in small bones and limited operative exposures during fracture fixation, plate osteosynthesis, corrective osteotomy stabilization, and selected reconstructive procedures. Relevant anatomical sites include the phalanges, metacarpals, selected carpal structures, metatarsals, and comparable small osseous regions treated with mini-fragment or small-fragment constructs. One hand stabilizes the drill body and trajectory while the other operates the crank. The instrument is used by orthopedic trauma surgeons, hand surgeons, foot and ankle surgeons, veterinary orthopedic specialists, and surgical teams working in hospitals, ambulatory operating rooms, trauma units, and specialty clinics. The listing identifies model PS-320.040 and includes three product images. Drill bits, guides, sleeves, depth gauges, taps, screws, plates, keys, adapters, and storage cases are separate components unless expressly included in the purchase order.

Exposed Gear Transmission and Micro-Pattern Control

The Micro Open Hand Drill converts manual crank movement into spindle rotation through an exposed stainless-steel gear train. As the operator turns the crank, the driving gear engages the corresponding spindle gear and rotates the attached orthopedic drill bit. The open architecture keeps the transmission visible during functional inspection, cleaning, lubrication, and movement assessment. Its compact frame reduces the space occupied around small fixation plates and short bone segments. The surgeon stabilizes the instrument with the supporting hand while the opposite hand supplies rotational movement. This arrangement separates axial guidance from crank input, allowing the drill to remain aligned with a plate hole or system-specific guide. The distal retention mechanism holds the selected bit concentrically and transfers rotational force to its cutting flutes. A properly matched guide establishes the entry point, supports the planned trajectory, and separates the rotating shaft from tendons, neurovascular structures, and other adjacent tissue. Manual operation provides tactile feedback as resistance changes between cortical and cancellous bone. Before operative use, the exposed gear teeth, crank, spindle, bit holder, and handle interfaces must be inspected for smooth engagement, secure alignment, and mechanical integrity. Gear binding, chuck slippage, eccentric rotation, corrosion, or deformation requires removal from the instrument set.

Small-Bone Fixation and Guided Drilling Workflow

The Micro Open Hand Drill is used for pilot-hole preparation during fixation of appropriately selected small-bone fractures and osteotomies. In phalangeal or metacarpal plate fixation, the fragments are reduced and temporarily stabilized before the selected plate is positioned against the cortex. A matching guide is introduced through the plate hole and seated at the planned entry point. The system-specific drill bit is secured in the handpiece, passed through the guide, and advanced through controlled crank rotation. The surgeon maintains axial alignment while monitoring tactile resistance as the cutting flutes cross the near cortex and enter cancellous bone. When bicortical purchase is planned, advancement continues toward the far cortex with restricted penetration beyond it. The channel is subsequently measured with a depth gauge, tapped when required by the screw design, and completed with the selected implant. The same sequence can support suitable metatarsal, small-foot, wrist, and veterinary small-bone fixation. Mini-fragment and small-fragment constructs use different drill-bit, guide, and screw relationships. The Micro Open Hand Drill provides rotational drive but does not determine the correct channel diameter or depth. Those parameters follow fracture morphology, plate design, screw core diameter, available bone stock, and the operative technique for the selected fixation system.

Catalog Model and Fixation-System Component Selection

Catalog model PS-320.040 identifies the Micro Open Hand Drill, while PS-OP-5828 is the Shopify inventory SKU shown on the product page. The live listing displays a size selector but does not present dimensional labels within the visible product information. The documented purchasing configuration is therefore identified by its SKU and catalog model. Clinical use depends on pairing the handpiece with a compatible drill bit, guide, sleeve, plate, screw, and depth gauge. Mini-fragment systems used in phalangeal or metacarpal fixation require smaller pilot channels than standard small-fragment constructs used in broader cortical bone. The chosen bit must correspond to the screw core diameter or specified gliding-hole dimension within the implant technique. Its shaft must seat concentrically within the drill’s retention mechanism without slippage or lateral movement. The guide bore must match the bit and engage the plate hole or exposed cortex securely. A depth gauge determines implant length after drilling; exposed bit length is not an acceptable substitute for channel measurement. Unicortical preparation terminates within the planned cortex, whereas bicortical fixation crosses the far cortex under controlled advancement. Bits, guides, taps, plates, screws, adapters, keys, and storage accessories are included only when documented in the quotation or order.

German Stainless Steel, Open-Gear Reprocessing, and Documentation

The Micro Open Hand Drill is manufactured from German stainless steel and incorporates the visible gear mechanism associated with its open pattern. Stainless-steel construction provides rigidity for transmitting rotational and axial force while supporting repeated inspection and validated reprocessing. The exposed transmission permits direct examination of the gear teeth and contacting surfaces for retained material, wear, corrosion, deformation, and impaired engagement. After use, personnel must clean the gear train, crank junction, spindle, bit-retention area, handle interfaces, and accessible recesses according to the manufacturer’s instructions. The drill should then be rinsed, completely dried, inspected, function-tested, packaged, and sterilized through the healthcare facility’s validated process. Authorized lubrication of moving surfaces must follow the supplied reprocessing guidance. Before packaging, the gear teeth should engage evenly, the crank should rotate without binding, and the spindle should remain aligned without excessive lateral play. Peak Surgicals supports CE and ISO 13485 documentation for institutional procurement assessment. FDA establishment registration, device listing, clearance, and approval are separate regulatory concepts; FDA-related wording must match the records applicable to the instrument and destination market. Hospitals and distributors should retain the SKU, catalog model, invoice, batch information, declarations, reprocessing instructions, and service documentation within their quality-management system.

SKU PS-OP-5828
Product Name Micro Open Hand Drill
Price $192.12 USD
Size/Gauge Variants Catalog model PS-320.040; live page includes a size selector without displayed dimensional labels
Instrument Category Micro-pattern manual orthopedic bone drill
Procedure Guided bone-channel preparation during small-bone fracture and osteotomy fixation
Material German stainless steel
Finish Metallic surgical instrument finish
Sterilization Reprocess according to the manufacturer’s instructions and the facility’s validated sterilization protocol
Instrument Classification Reusable manual orthopedic surgical instrument
Reusable Yes
Certifications CE and ISO 13485 procurement documentation; FDA-related records supplied according to applicable market requirements
Warranty 30-day money-back guarantee under the published store policy
MOQ One instrument for standard online orders
OEM / Custom Orders OEM, private-label, and institutional requirements are handled through a written quotation
After-Sale Service Order, documentation, and product-support assistance through Peak Surgicals customer service

How does the Micro Open Hand Drill differ from the Micro Hand Drill with closed gears?
The Micro Open Hand Drill exposes its gear train for direct visual access. A Micro Hand Drill with closed gears contains the transmission within a surrounding housing. Both patterns transfer manual crank movement to a spindle and retained orthopedic drill bit. The open configuration allows direct inspection and cleaning of visible gear teeth. The closed pattern presents an integrated casing around the transmission. Selection depends on the surgeon’s handling preference, the facility’s reprocessing workflow, and compatibility with the intended drilling components.

How should drill-bit size be selected for this micro drill?
The bit must correspond to the screw and plate system used for the planned fixation. Phalangeal, metacarpal, carpal, and metatarsal constructs can require different pilot-hole dimensions. A threaded pilot channel follows the screw core diameter, while a gliding hole follows the fixation system’s specified dimension. The guide bore must match the selected bit and seat securely within the plate hole or against the cortex. The bit must remain concentric in the Micro Open Hand Drill without slipping during rotation. Final screw length is selected after channel depth is measured with a compatible depth gauge.

What do CE, ISO 13485, and FDA references mean for procurement?
CE documentation supports assessment against applicable European medical-device requirements. ISO 13485 concerns the manufacturer’s medical-device quality-management system rather than serving as individual product approval. FDA establishment registration, device listing, clearance, and approval carry different regulatory meanings. The Micro Open Hand Drill should not be called FDA approved without a supporting product-specific approval record. United States purchasing teams should evaluate the documentation relevant to the device classification and supply route. Peak Surgicals can provide available commercial and regulatory records for institutional review before purchase.

How is the exposed crank-and-gear mechanism operated intraoperatively?
The surgeon stabilizes the Micro Open Hand Drill with one hand and turns its crank with the other. Crank movement rotates the exposed gear train, which transfers motion to the spindle and attached bit. The supporting hand maintains alignment with the selected guide and planned screw axis. Axial pressure is applied through the guide rather than laterally against the rotating shaft. The operator monitors resistance as the bit passes through cortical and cancellous bone. Before use, the gears, crank, spindle, and bit holder must move securely without binding, slippage, damage, or excessive play.

What should an operating-room team assess before sterilizing and purchasing the drill?
The procurement team should confirm SKU PS-OP-5828, catalog model PS-320.040, quantity, and compatibility with the intended fixation components. The facility must obtain the manufacturer’s cleaning and sterilization instructions before clinical use. Reprocessing personnel should clean and inspect each visible gear tooth, junction, recess, spindle surface, and bit-retention area. The Micro Open Hand Drill requires a functional movement test before packaging for the validated sterilization cycle. Drill bits, guides, depth gauges, taps, plates, screws, and cases should be ordered separately unless listed in the quotation. Product, batch, invoice, regulatory, maintenance, and service records should remain within the institution’s quality documentation.