Silicone Oil Infusion Line 23G for Tocar
EUDAMEDFDA UDIClass IIa (EU MDR)
by Aktive Srl
Identity
- Trade Name
- Silicone Oil Infusion Line 23G for Tocar EUDAMEDFDA UDI
- Generic Name
- Ophthalmic irrigation/infusion/aspiration tubing, single-use FDA UDI
- Device Name
- Infusion Cannula /Linea Silicone/ Mantenitori C.A._ Infusion Cannula/Silicone Infusion Line/Mantainer C.A. EUDAMEDSilicone Oil Infusion Line 23G for Tocar FDA UDI
- Model / Reference
- Infusion Cannula /Linea Silicone/ Mantenitori C.A._ Infusion Cannula/Silicone Infusion Line/Mantainer C.A. EUDAMEDAK-0357/N EUDAMEDFDA UDI
- Description
- Silicone Oil Infusion Line 23G for Tocar FDA UDI
Identifiers
- Catalog Number
- AK-0357/N FDA UDI
- Primary DI / UDI-DI
- 08052276019639 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0001ID11KP EUDAMED
- Unit of Use DI
- 08058340220086 EUDAMED
- FDA Product Code
- HMX FDA UDI
- EMDN Code
- Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic irrigation/infusion/aspiration tubing, 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
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use
Silicone Oil Infusion Line 23G for Tocar by Aktive Srl — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.
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- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- SURGISTAR — Surgistar Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8052276FT0001ID11KP | 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 85570a33-5029-414d-a015-c94afa2f80ad 61 fields · synced Jun 18, 2026
- FDA UDI a33bc3f3-0c1b-49ff-aced-61b86fa73e93 36 fields · synced May 30, 2026