Identity
- Device Name
- 23ga ACTU8 Tewari (T2) Forceps EUDAMED
- Model / Reference
- VS0742.23 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00810123481156 EUDAMED
- Basic UDI-DI
- B-00810123481156 EUDAMED
- EMDN Code
- Q020599 RETINAL DETACHMENT DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
23ga ACTU8 Tewari (T2) Forceps by Vortex Surgical, Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00810123481156 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Vortex Surgical Inc
- EUDAMED SRN
- US-MF-000022888
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED 465d9d0b-258d-40d0-a3c2-835f3bcf58cd 61 fields · synced Aug 4, 2026