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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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Rippenbandage — 2 UDI-DI variants, MDR (John GmbH)

MD Atlas
John GmbH

Data from EUDAMED, last updated May 23, 2026

Rippenbandage

42519921RippBOBX

2 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: John GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42519921RippBOBX
Device name: Rippenbandage
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: John GmbH
SRN: DE-MF-000012375
Country: Germany
Email: hugo.dewit@johngmbh.com
Phone: +49 36923 8388-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K7744CY5M17N42Q1JG0A8VW5

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

BANDAGE-04050-D-M-104251992197001
BANDAGE-04050-H-M-104251992197018