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Gimmi

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref T.1002.99

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Product for cleaning and storage EUDAMED
STERILIZATION WIRE BASKETS FOR 1 ENDOSCOPE Ø 2 - 10 MM 455 X 80 X 52 MM FDA UDI
Model / Reference
T.1002.99 EUDAMEDFDA UDI
Description
STERILIZATION WIRE BASKETS FOR 1 ENDOSCOPE Ø 2 - 10 MM 455 X 80 X 52 MM FDA UDI

Identifiers

Primary DI / UDI-DI
04049047099093 EUDAMEDFDA UDI
Basic UDI-DI
4049047SAA08ABA27DRED4 EUDAMED
Direct Marketing DI
04049047099093 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Device sterilization/disinfection container, reusable

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

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (2)

  • FDA UDI 78ed7428-c9a4-4801-aa41-5c2911fd137f 34 fields · synced Jun 19, 2026
  • EUDAMED 7884757d-0f1b-4a76-afdc-262ae6f2b854 61 fields · synced Jun 19, 2026