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Retinal Tip 20G Microscissors Straight
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref AK-1669Model Retinal Tip/Pinzetta Retinica
by Aktive Srl
Identity
- Trade Name
- Retinal Tip 20G Microscissors Straight EUDAMEDFDA UDI
- Generic Name
- Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI
- Device Name
- Retinal Tip/Pinzetta Retinica EUDAMEDRetinal Tip 20G Microscissors Straight FDA UDI
- Model / Reference
- Retinal Tip/Pinzetta Retinica EUDAMEDAK-1669 EUDAMEDFDA UDI
- Description
- Retinal Tip 20G Microscissors Straight FDA UDI
Identifiers
- Catalog Number
- AK-1669 FDA UDI
- Primary DI / UDI-DI
- 08052276028143 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0002ID6CR EUDAMED
- Unit of Use DI
- 08056477550618 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 20G Microscissors Straight 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 7549a4ca-60e7-4453-b81c-4ea302070282 61 fields · synced Jun 18, 2026
- FDA UDI 74f5de09-fe1a-43f2-9a94-5aa00bd5f2dc 36 fields · synced May 29, 2026