← Back to catalogue
Side Port Knife 0.6 mm Angled
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref P-06/AModel Knife/Bisturi
by Aktive Srl
Identity
- Trade Name
- Side Port Knife 0.6 mm Angled EUDAMEDFDA UDI
- Generic Name
- Ophthalmic knife, single-use FDA UDI
- Device Name
- Knife/Bisturi EUDAMEDSide Port Knife 0.6 mm Angled FDA UDI
- Model / Reference
- Knife/Bisturi EUDAMEDP-06/A EUDAMEDFDA UDI
- Description
- Side Port Knife 0.6 mm Angled FDA UDI
Identifiers
- Catalog Number
- P-06/A FDA UDI
- Primary DI / UDI-DI
- 08052276033970 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0002ID2CH EUDAMED
- Unit of Use DI
- 08056477557785 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 — 0.6 Millimeter FDA UDI
Side Port Knife 0.6 mm 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aktive Srl
- EUDAMED SRN
- IT-MF-000007813
Sources (2)
- EUDAMED 2013ea09-030b-4499-94f3-74497bf18fc2 61 fields · synced Jun 18, 2026
- FDA UDI ff022571-bce6-46ee-a81c-fb4a3be62b87 36 fields · synced May 30, 2026