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Crescent Knife 2.0 mm Bevel Up Angled
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref C-20/AModel Knife/Bisturi
by Aktive Srl
Identity
- Trade Name
- Crescent Knife 2.0 mm Bevel Up Angled EUDAMEDFDA UDI
- Generic Name
- Ophthalmic knife, single-use FDA UDI
- Device Name
- Knife/Bisturi EUDAMEDCrescent Knife 2.0 mm Bevel Up Angled FDA UDI
- Model / Reference
- Knife/Bisturi EUDAMEDC-20/A EUDAMEDFDA UDI
- Description
- Crescent Knife 2.0 mm Bevel Up Angled FDA UDI
Identifiers
- Catalog Number
- C-20/A FDA UDI
- Primary DI / UDI-DI
- 08052276029652 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0002ID2CH EUDAMED
- Unit of Use DI
- 08056477557594 EUDAMED
- FDA Product Code
- HNN FDA UDI
- EMDN Code
- Q021109 OPHTHALMIC SURGERY SPATULAS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic knife, 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
Dimensions & Sizes
- Size
- Length — 2.0 Millimeter FDA UDI
Crescent Knife 2.0 mm Bevel Up Angled 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 | 8052276FT0002ID2CH | 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 e1b439e9-ca78-473a-8d46-4a98acb7e410 61 fields · synced Jul 30, 2026
- FDA UDI 3ea22840-47d5-43fb-bf39-2b1847ae7d6d 36 fields · synced May 30, 2026