Gimmi

FDA UDI

Class II (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name: Gimmi FDA UDI
Generic Name: Laparoscopic access cannula seal, single-use FDA UDI
Device Name: SEALING CAP, RED, WITH HOLE 5 MM TROCAR 6 - 6.5 MM Ø FDA UDI
Model / Reference: T.9050.13 FDA UDI
Description: SEALING CAP, RED, WITH HOLE 5 MM TROCAR 6 - 6.5 MM Ø FDA UDI

Identifiers

Catalog Number: T.9050.13 FDA UDI
Primary DI / UDI-DI: 04049047557845 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Laparoscopic access cannula seal, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic access cannula seal, single-use

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

Similar devices

Also classified as Laparoscopic access cannula seal, single-use.

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Disposable valve for trocar D=3, 5mm (x3) — Medica Corp. · Class II
Convertible Trocar System — APPLIED MEDICAL RESOURCES CORP. · Class II
GloShield — JACKSON MEDICAL LLC · Class I
Morcellator — Karl Storz GmbH & Co. KG · Class II
Disposable valves for trocar Ø 3 mm — Medica Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Gimmi GmbH

Sources (1)

FDA UDI 654f5a09-2967-4116-9ff5-5d9a7636fb37 35 fields · synced Jun 8, 2026