Gimmi T.8002.06

Gimmi T.8002.06 is a Class II device made by Gimmi GmbH, listed in FDA GUDID since 5 May 2017 (UDI-DI 04049047102199), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04049047102199 UDI-DI	Date5 May 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04049047102199

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Gimmi
Generic name: Laparoscopic access cannula, reusable
Model / Ref / Catalog: T.8002.06
Description: TROCAR SLEEVE WITH SILICONEVALVE AND PYRAMIDAL TIP, 5.5 MM CONSISTING OF:

Primary DI / UDI-DI: 04049047102199
FDA product code: GCJ
GMDN term: Laparoscopic access cannula, reusable

Device class: Class II
Regulation number: 876.1500
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use

Other properties (13, all answered No)