Mantainer anterior chamber 25G
EUDAMEDFDA UDIClass IIa (EU MDR)
by Aktive Srl
Identity
- Trade Name
- Mantainer anterior chamber 25G 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. EUDAMEDMantainer anterior chamber 25G FDA UDI
- Model / Reference
- Infusion Cannula /Linea Silicone/ Mantenitori C.A._ Infusion Cannula/Silicone Infusion Line/Mantainer C.A. EUDAMEDAK-0332 EUDAMEDFDA UDI
- Description
- Mantainer anterior chamber 25G FDA UDI
Identifiers
- Catalog Number
- AK-0332 FDA UDI
- Primary DI / UDI-DI
- 08052276019455 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0001ID11KP EUDAMED
- Unit of Use DI
- 08056477554999 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
Mantainer anterior chamber 25G by Aktive Srl — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.
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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 007ce7e1-a521-45fc-a10b-1dec33597ff6 61 fields · synced Jun 18, 2026
- FDA UDI 52c9dc84-4774-4800-bc64-6c1eb75b1f7d 36 fields · synced May 30, 2026