Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- Laparoscopic access cannula seal, single-use FDA UDI
- Device Name
- SEALING CAP, GREY, WITH HOLE 7 MM TROCAR 8 MM Ø FDA UDI
- Model / Reference
- T.9110.09 FDA UDI
- Description
- SEALING CAP, GREY, WITH HOLE 7 MM TROCAR 8 MM Ø FDA UDI
Identifiers
- Catalog Number
- T.9110.09 FDA UDI
- Primary DI / UDI-DI
- 04049047637936 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
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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- 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 bc40b905-17f6-4a8f-b8e3-951619ec2da4 35 fields · synced May 31, 2026