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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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Instruments, orthopaedic surgeries of… — 7 UDI-DI variants, MDR

MD Atlas
In2Bones SAS

Data from EUDAMED, last updated May 19, 2026

Instruments, orthopaedic surgeries of the upper and lower extremities

3701337641146Y

7 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: In2Bones SAS

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 3701337641146Y
Device name: Instruments, orthopaedic surgeries of the upper and lower extremities
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: In2Bones SAS
SRN: FR-MF-000005246
Country: France
Email: in2bfr.qualite@conmed.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KQT4SFG5T8FK628W5RJQSCN8

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

IBS™03760225713112
IBS™03760225713129
In2Bones03760225710951
In2Bones03760225717257
NEOFUSE03760225717141
NEOFUSE03760225717127
TRIWAY03760225718858