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Gimmi

FDA UDI

Class I (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Endometrial biopsy curette FDA UDI
Device Name
MIKRODISECTOMY CURETTE CERVICAL FIG. 0, ANGLED, BACKWARD LENGTH 210 MM, NOT FOR NEURO AND CARDIO FDA UDI
Model / Reference
GK.2014.01 FDA UDI
Description
MIKRODISECTOMY CURETTE CERVICAL FIG. 0, ANGLED, BACKWARD LENGTH 210 MM, NOT FOR NEURO AND CARDIO FDA UDI

Identifiers

Catalog Number
GK.2014.01 FDA UDI
Primary DI / UDI-DI
04049047701798 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Endometrial biopsy curette 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: Endometrial biopsy curette

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

Similar devices

Also classified as Endometrial biopsy curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI 51954063-0f6b-45d2-8e90-1863f2701407 35 fields · synced May 30, 2026