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MY SCREW Ø2.5 Lg 22
EUDAMEDClass IIb (EU MDR)
Ref 38.88.22Model MY SCREW
by Ortho Cape
Identity
- Trade Name
- MY SCREW Ø2.5 Lg 22 EUDAMED
- Device Name
- MY SCREW Ø2.5 Lg 22mm EUDAMED
- Model / Reference
- MY SCREW EUDAMED38.88.22 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760347451404 EUDAMED
- Basic UDI-DI
- B-03760347451404 EUDAMED
- EMDN Code
- P09120603 CANNULATED SCREWS EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
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
MY SCREW Ø2.5 Lg 22 by Ortho Cape — Class IIb — 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-03760347451404 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Ortho Cape
- EUDAMED SRN
- FR-MF-000028862
Sources (1)
- EUDAMED 652b1b4c-1ca3-4441-8336-bf0744546eeb 61 fields · synced Sep 17, 2026