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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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Positionierungshilfen — 214 UDI-DI variants, MDR (OBA AG)

MD Atlas
OBA AG

Data from EUDAMED, last updated May 23, 2026

Positionierungshilfen

76303184POSYZ

214 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: OBA AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76303184POSYZ
Device name: Positionierungshilfen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: OBA AG
SRN: CH-MF-000037383
Country: Switzerland
Email: info@oba.ch

Authorised representative

Name: ANNIE BAUER CONFORT
SRN: FR-AR-000037165
Country: France
Phone: +33493229475

Variants by status

UDI-DI variants

214 UDI-DI variants

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Applied filters

basicUdiUlid01HNJH5MGW0FEB6ZN5E3AHJPSB

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

3043.000.038.0107630318405551
3043.000.038.9007630318405568
RG35.9007630318405674
RG35.0107630318405667
1002.00207630318405957
60007630318406039
1002.00307630318405964
1002.00107630318405940
3061.50307630318406077
3061.50107630318406060
3061.101.9007630318405469
3061.50207630318406053
3061.10207630318406046
Moovecare07630318405476

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