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Gimmi

FDA UDI

Class I (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Amputation knife FDA UDI
Device Name
LANGENBECK RESECTION KNIFE POINTED LENGTH OF BLADE 55 MM FDA UDI
Model / Reference
AA.0868.02 FDA UDI
Description
LANGENBECK RESECTION KNIFE POINTED LENGTH OF BLADE 55 MM FDA UDI

Identifiers

Catalog Number
AA.0868.02 FDA UDI
Primary DI / UDI-DI
04049047000365 FDA UDI
FDA Product Code
EMF FDA UDI
GMDN Term
Amputation knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Amputation knife

Gimmi by Gimmi GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amputation knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI c7e855d0-ba32-436e-902d-327ae72097d4 35 fields · synced Jun 6, 2026