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Karl Schumacher

FDA UDI

Class I (US FDA UDI)

by Karl Schumacher Dental, Llc

Identity

Trade Name
Karl Schumacher FDA UDI
Generic Name
Tooth extraction forceps FDA UDI
Device Name
Up Mlr Apical Rtntn Frcps #1167 FDA UDI
Model / Reference
EXF1167 FDA UDI
Description
Up Mlr Apical Rtntn Frcps #1167 FDA UDI

Identifiers

Primary DI / UDI-DI
00842517110038 FDA UDI
FDA Product Code
EMG FDA UDI
GMDN Term
Tooth extraction forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tooth extraction forceps

Karl Schumacher by Karl Schumacher Dental, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tooth extraction forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36527823-556f-40c0-913e-a1e09c180265 34 fields · synced May 31, 2026