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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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DIAM, Packaging — 4 UDI-DI variants, MDR (Companion Spine France SAS)

MD Atlas
Companion Spine France SAS

Data from EUDAMED, last updated May 19, 2026

DIAM, Packaging

37015213FDMN00104S

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: Companion Spine France SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37015213FDMN00104S
Device name: DIAM, Packaging
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: Companion Spine France SAS
SRN: FR-MF-000013875
Country: France
Email: contact@companion-spine.com
Phone: +33 5 32 26 25 70

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HNFF021CYWPT6SMQAQKWK6YJ

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

DIAM, Outer Case03701521300149
DIAM, Outer Case Lid03701521300156
DIAM, Upper Instrument Tray03701521300415
DIAM, Upper Instrument Tray03701521300163