Identity
- Device Name
- 23ga ACTU8 Adaptive Forceps EUDAMED
- Model / Reference
- VS0740.23 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00810123481125 EUDAMED
- Basic UDI-DI
- B-00810123481125 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 Adaptive 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-00810123481125 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Vortex Surgical Inc
- EUDAMED SRN
- US-MF-000022888
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED f40f1fd4-5c58-46a1-8307-36c9785d44a7 61 fields · synced Jun 17, 2026