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Puncher

FDA UDI

Class I (US FDA UDI)

by MPS Micro Precision Systems AG

Identity

Trade Name
Puncher FDA UDI
Generic Name
Bone lever/elevator, reusable FDA UDI
Device Name
A hand-held instrument used to, as soon as the femoral implant has been loosed by the chisel blade, for punching out the femoral implant. The extremity is applied proximal onto onto the femoral anterior flange for a stable and safe extraction.This is a reusable device. FDA UDI
Model / Reference
T14586 FDA UDI
Description
A hand-held instrument used to, as soon as the femoral implant has been loosed by the chisel blade, for punching out the femoral implant. The extremity is applied proximal onto onto the femoral anterior flange for a stable and safe extraction.This is a reusable device. FDA UDI

Identifiers

Catalog Number
T14586 FDA UDI
Primary DI / UDI-DI
07640187910506 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone lever/elevator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone lever/elevator, reusable

Puncher by MPS Micro Precision Systems AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone lever/elevator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 562b0167-650c-45bd-974e-fdc5da5714ee 35 fields · synced May 30, 2026