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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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Moorkissen — 5 UDI-DI variants, MDR (bb med. product GmbH)

MD Atlas
bb med. product GmbH

Data from EUDAMED, last updated May 23, 2026

Moorkissen

4007944bbm30177

5 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: bb med. product GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4007944bbm30177
Device name: Moorkissen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 8, 2021

Manufacturer & authorised representative

Manufacturer

Name: bb med. product GmbH
SRN: DE-MF-000005155
Country: Germany
Email: info@bb-kalkar.de
Phone: +49 2824 20830

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FKZQAKSRTHYNBQZDKR47EZPR

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

1182130100204007944003698
1182130100604007944003711
1025030100604007944003582
1182130100104007944003704
1025030100504007944003575