← Back to catalogue

PIN Drill Guide CL

FDA UDI

Class III (US FDA UDI)

by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Identity

Trade Name
PIN Drill Guide CL FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
Reusable Surgical Tool FDA UDI
Model / Reference
36878 FDA UDI
Description
Reusable Surgical Tool FDA UDI

Identifiers

Primary DI / UDI-DI
09008737368784 FDA UDI
PMA Number
P000025 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant template, reusable

PIN Drill Guide CL by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI dbd2f620-820c-4ef8-a16b-dd90470227ca 35 fields · synced May 31, 2026