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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Glenoid instrumentation — 4 UDI-DI variants, MDR (S.B.M. SAS)

MD Atlas
S.B.M. SAS

Data from EUDAMED, last updated May 19, 2026

Glenoid instrumentation

376015400DT2021012TV

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: S.B.M. SAS

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 376015400DT2021012TV
Device name: Glenoid instrumentation
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: S.B.M. SAS
SRN: FR-MF-000000214
Country: France
Email: contact@sbm-fr.com
Phone: +33 5 62 42 21 01

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HD6PWP4TQRZV3A0C2MQPCTDS

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

GLE900040703760304681011
GLE900042803760304681097
GLE900042603760304681059
GLE900042703760304681066