Identity
- Trade Name
- ALPHAPORT EUDAMEDGimmi FDA UDI
- Generic Name
- Laparoscopic access cannula, reusable FDA UDI
- Device Name
- Trocar Systems & Accessories EUDAMEDREDUCER 12.5/11/10 MM - 5.5 MM, SLIDING VERSION FOR ALL TROCAR SLEEVES FDA UDI
- Model / Reference
- T.8024.50 EUDAMEDFDA UDI
- Description
- REDUCER 12.5/11/10 MM - 5.5 MM, SLIDING VERSION FOR ALL TROCAR SLEEVES FDA UDI
Identifiers
- Catalog Number
- T.8024.50 FDA UDI
- Primary DI / UDI-DI
- 04049047123811 EUDAMEDFDA UDI
- Basic UDI-DI
- 4049047LFP09BJA27DREVZ EUDAMED
- Direct Marketing DI
- 04049047123811 EUDAMED
- FDA Product Code
- GCJ FDA UDI
- EMDN Code
- L031280 SURGICAL TROCAR, REUSABLE - ACCESSORIES EUDAMED
- GMDN Term
- Laparoscopic access cannula, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 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
Yes
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
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, reusable
Gimmi by Gimmi GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Laparoscopic access cannula, reusable.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Gimmi GmbH
Sources (2)
- FDA UDI 09893275-850f-43b9-89e6-42f1d2e3cc57 35 fields · synced Jun 19, 2026
- EUDAMED d7606ec9-6e34-4165-a738-368050ac453c 61 fields · synced Jun 19, 2026