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Gimmi

FDA UDI

Class I (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Surgical A/V-shaped microvessel clamp FDA UDI
Device Name
MICRO ARTERY CLAMP SINGLE TYPE 4, 1.5 - 3.3 MM LENGTH 24 MM FDA UDI
Model / Reference
CC.1158.15 FDA UDI
Description
MICRO ARTERY CLAMP SINGLE TYPE 4, 1.5 - 3.3 MM LENGTH 24 MM FDA UDI

Identifiers

Catalog Number
CC.1158.15 FDA UDI
Primary DI / UDI-DI
04049047694793 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Surgical A/V-shaped microvessel clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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: Surgical A/V-shaped microvessel clamp

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

Similar devices

Also classified as Surgical A/V-shaped microvessel clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI dcf656dc-0685-404a-8404-9e2a03be3a37 35 fields · synced May 30, 2026