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Gimmi

FDA UDI

Class II (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
AUTOMATIC TROCAR SLEEVE 7 MM WITH STOP-COCK FOR INSUFFLATION AND TROCAR MANDRIN WITH PYRAMIDAL TIP, COMPLETE FDA UDI
Model / Reference
T.8013.07 FDA UDI
Description
AUTOMATIC TROCAR SLEEVE 7 MM WITH STOP-COCK FOR INSUFFLATION AND TROCAR MANDRIN WITH PYRAMIDAL TIP, COMPLETE FDA UDI

Identifiers

Catalog Number
T.8013.07 FDA UDI
Primary DI / UDI-DI
04049047103714 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, reusable 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic access cannula, reusable

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

Similar devices

Also classified as Laparoscopic access cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI 26444f99-f31f-4ff1-b72c-0c301541c590 35 fields · synced Jun 1, 2026