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55° Rotary microscissor 20G only Tip
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref AK-1651(S)Model Retinal Tip/Pinzetta Retinica
by Aktive Srl
Identity
- Trade Name
- 55° Rotary microscissor 20G only Tip EUDAMEDFDA UDI
- Generic Name
- Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI
- Device Name
- Retinal Tip/Pinzetta Retinica EUDAMED55° Rotary microscissor 20G only Tip FDA UDI
- Model / Reference
- Retinal Tip/Pinzetta Retinica EUDAMEDAK-1651(S) EUDAMEDFDA UDI
- Description
- 55° Rotary microscissor 20G only Tip FDA UDI
Identifiers
- Catalog Number
- AK-1651(S) FDA UDI
- Primary DI / UDI-DI
- 08052276028044 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0002ID6CR EUDAMED
- Unit of Use DI
- 08052276000347 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
55° Rotary microscissor 20G only Tip 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 a0c0e0e6-2866-4b32-931f-f23d2e88b2d3 61 fields · synced Aug 2, 2026
- FDA UDI f6acb085-99f1-45a3-a5f7-595cac0e1923 36 fields · synced May 30, 2026