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GlenoTech®
EUDAMEDClass I (EU MDR)
Ref GLE9000410Model Aiming device
by S.b.m. Sas
Identity
- Trade Name
- GlenoTech® EUDAMED
- Device Name
- Glenoid instrumentation EUDAMED
- Model / Reference
- Aiming device EUDAMEDGLE9000410 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760304681035 EUDAMED
- Basic UDI-DI
- 376015400DT2021011TT EUDAMED
- EMDN Code
- L091099 OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Category: Surgical implant template, reusable
GlenoTech® by S.b.m. Sas — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | 376015400DT2021011TT | Class I | Active |
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Manufacturer
- Manufacturer
- S.b.m. Sas
- EUDAMED SRN
- FR-MF-000000214
Sources (1)
- EUDAMED b5bb9744-d7d0-4e29-821f-d2dae81cb620 61 fields · synced Jun 9, 2026