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Retinal Tip 25G Microscissors Curved
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref AK-1683Model Retinal Tip/Pinzetta Retinica
by Aktive Srl
Identity
- Trade Name
- Retinal Tip 25G Microscissors Curved EUDAMEDFDA UDI
- Generic Name
- Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI
- Device Name
- Retinal Tip/Pinzetta Retinica EUDAMEDRetinal Tip 25G Microscissors Curved FDA UDI
- Model / Reference
- Retinal Tip/Pinzetta Retinica EUDAMEDAK-1683 EUDAMEDFDA UDI
- Description
- Retinal Tip 25G Microscissors Curved FDA UDI
Identifiers
- Catalog Number
- AK-1683 FDA UDI
- Primary DI / UDI-DI
- 08052276028372 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0002ID6CR EUDAMED
- Unit of Use DI
- 08056477550724 EUDAMED
- FDA Product Code
- HNF FDA UDI
- EMDN Code
- Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic soft-tissue surgical forceps probe-tip, 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
Retinal Tip 25G Microscissors Curved 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 | 8052276FT0002ID6CR | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Aktive Srl
- EUDAMED SRN
- IT-MF-000007813
Sources (2)
- EUDAMED da7d3ee0-e108-47d0-ac71-f914ee3d8133 61 fields · synced Jul 27, 2026
- FDA UDI 09382b36-b03c-4093-96e4-1ea83c56f127 36 fields · synced May 30, 2026