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Subtenon's Cannula 19G 25mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 5176Model Needles and Cannulae / Aghi e Cannule
by Aktive Srl
Identity
- Trade Name
- Subtenon's Cannula 19G 25mm EUDAMEDFDA UDI
- Generic Name
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
- Device Name
- Needles and Cannulae / Aghi e Cannule EUDAMEDSubtenon's Cannula 19G 25mm FDA UDI
- Model / Reference
- Needles and Cannulae / Aghi e Cannule EUDAMED5176 EUDAMEDFDA UDI
- Description
- Subtenon's Cannula 19G 25mm FDA UDI
Identifiers
- Catalog Number
- 5176 FDA UDI
- Primary DI / UDI-DI
- 08052276015617 EUDAMEDFDA UDI
- Basic UDI-DI
- 8052276FT0001ID10KM EUDAMED
- Unit of Use DI
- 08056477558096 EUDAMED
- FDA Product Code
- HMX FDA UDI
- EMDN Code
- Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, 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
Subtenon's Cannula 19G 25mm 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 | 8052276FT0001ID10KM | 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 b46c60f9-37c0-4de6-9e82-cdd0057bcaa3 61 fields · synced Jun 8, 2026
- FDA UDI a15550fd-2121-4652-870b-098624eb7f07 36 fields · synced May 30, 2026