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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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Articulatory Orthoses — 12 UDI-DI variants, MDR (Baumann Ed.)

MD Atlas
Baumann Ed.

Data from EUDAMED, last updated May 19, 2026

Articulatory Orthoses

952538593orthesisV4

12 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: Baumann Ed.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 952538593orthesisV4
Device name: Articulatory Orthoses
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: Baumann Ed.
SRN: FR-MF-000049737
Country: France
Email: contact@baumann-ed.com
Phone: 0621666926

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01K6WDJP9J0370ECJTZBXTJP9G

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

CHAJA T103770040164006
CHAJA T203770040164143
FAVA T203770040164167
FAVA T103770040164020
KAGARA T203770040164181
KAGARA T103770040164044
PABAMA03770040164013
PABAMA03770040164150
SAZA T203770040164174
SAZA T103770040164037
TADANALA T203770040164198
TADANALA T103770040164051