← Back to catalogue
TWEEZER GRIP 25G (45mm)
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref AK-1671GXXLModel TWEEZER / PINZETTA TWEEZER
by Aktive Srl
Identity
- Trade Name
- TWEEZER GRIP 25G (45mm) EUDAMEDFDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
- Device Name
- TWEEZER / PINZETTA TWEEZER EUDAMEDTWEEZER GRIP 25G (45mm) FDA UDI
- Model / Reference
- TWEEZER / PINZETTA TWEEZER EUDAMEDAK-1671GXXL EUDAMEDFDA UDI
- Description
- TWEEZER GRIP 25G (45mm) FDA UDI
Identifiers
- Catalog Number
- AK-1671GXXL FDA UDI
- Primary DI / UDI-DI
- 08052276028242 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0002ID1CF EUDAMED
- Unit of Use DI
- 08052276000453 EUDAMED
- FDA Product Code
- HNR FDA UDI
- EMDN Code
- Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
TWEEZER GRIP 25G (45mm) by Aktive Srl — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8052276FT0002ID1CF | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aktive Srl
- EUDAMED SRN
- IT-MF-000007813
Sources (2)
- EUDAMED 4c99ca8c-3185-45ed-b9ff-77a4d6d18cfa 61 fields · synced Jun 17, 2026
- FDA UDI 59ffc892-e542-4c6c-9dda-041982fd7db7 36 fields · synced May 30, 2026