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GlenoTech®

EUDAMED

Class I (EU MDR)

Ref GLE9000411Model Aiming device

by S.b.m. Sas

Identity

Trade Name
GlenoTech® EUDAMED
Device Name
Glenoid instrumentation EUDAMED
Model / Reference
Aiming device EUDAMED
GLE9000411 EUDAMED

Identifiers

Primary DI / UDI-DI
03760304681042 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

GlenoTech® by S.b.m. Sas — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
S.b.m. Sas
EUDAMED SRN
FR-MF-000000214

Sources (1)

  • EUDAMED 5138e6db-676f-458e-8722-a0d525d3aab3 61 fields · synced Jun 9, 2026