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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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Bone tap for ACL reconstruction — 5 UDI-DI variants, MDR (S.B.M. SAS)

MD Atlas
S.B.M. SAS

Data from EUDAMED, last updated May 19, 2026

Bone tap for ACL reconstruction

376015400DT2019046VT

5 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: 376015400DT2019046VT
Device name: Bone tap for ACL reconstruction
Device model: Bone tap
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 20, 2023

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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H5SKN63MWRYNN1JYDASQDH3W

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

11002610403760154007917
25641203760154007986
LIG900029603760154005722
LIG900009303760154002264
LIG900016903760154002271