← Back to catalogue
Vitrectomy pack 23 G
EUDAMEDClass IIa (EU MDR)
Ref VV630213BBModel MD0105.17 Vitrectomy Packs OS4 Single Use
Identity
- Trade Name
- Vitrectomy pack 23 G EUDAMED
- Model / Reference
- MD0105.17 Vitrectomy Packs OS4 Single Use EUDAMEDVV630213BB EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07630003912975 EUDAMED
- Basic UDI-DI
- 76300039MD010517TD EUDAMED
- EMDN Code
- Q020402 POSTERIOR VITRECTOMY SETS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
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
Vitrectomy pack 23 G by Oertli Instrumente Ag — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 76300039MD010517TD | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Oertli Instrumente AG
- EUDAMED SRN
- CH-MF-000016175
- Authorised Representative
- Oertli Ophthalmedic Österreich GmbH AT-AR-000003554
Sources (1)
- EUDAMED ef8c0056-1f86-4655-bbe5-48cf0ef2d32b 61 fields · synced Jul 14, 2026