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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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2-Channel-Ring-Applicator CT/MR — 1 UDI-DI variant, MDD

MD Atlas
BEBIG Medical GmbH

Data from EUDAMED, last updated May 30, 2026

2-Channel-Ring-Applicator CT/MR

B-04065983002218

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: BEBIG Medical GmbH

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2254550CE01
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DEKRA Certification B.V. (0344)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-04065983002218
Device name: 2-Channel-Ring-Applicator CT/MR
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Apr 28, 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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Applied filters

basicUdiUlid01KQA2J7P3GB6DCE3X19M232MS

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

2-Channel-Ring-Applicator CT/MR, 45°, D=35mm04065983002218