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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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M05 01321 — 6 UDI-DI variants, MDR (In2Bones SAS)

MD Atlas
In2Bones SAS

Data from EUDAMED, last updated May 19, 2026

M05 01321

3701337619517R

6 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3701337619517R
Device name: —
Device model: M05 01321
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KBZ9XBM3WV36V1T5QCGXMGM2

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

QUANTUM03701337607371
QUANTUM03701337607357
QUANTUM03701337607364
QUANTUM03701337607401
QUANTUM03701337607333
QUANTUM03701337607388