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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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Set of X-Ray Markers — 1 UDI-DI variant, MDR (BEBIG Medical GmbH)

MD Atlas
BEBIG Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Set of X-Ray Markers

40659830030BCC

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: BEBIG Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40659830030BCC
Device name: Set of X-Ray Markers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: BEBIG Medical GmbH
SRN: DE-MF-000012644
Country: Germany
Email: sales@bebigmedical.com
Phone: +49 3 094 87 88 810

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KP65JPBV4YB6KFK8VFKJZ205

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

Set of X-Ray Markers; L=325mm; Code=01-0204065983001129