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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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KANJO B-protect — 6 UDI-DI variants, MDR (DIETZ GmbH)

MD Atlas
DIETZ GmbH

Data from EUDAMED, last updated May 23, 2026

KANJO B-protect

42602416851BWL000017T

6 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: DIETZ GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42602416851BWL000017T
Device name: KANJO B-protect
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 20, 2024

Manufacturer & authorised representative

Manufacturer

Name: DIETZ GmbH
SRN: DE-MF-000009121
Country: Germany
Email: info@dietz-group.de
Phone: +49 7248 9186 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JD4TZZZ51QDTVFXAT25K8AMT

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

750/3004260241684544
750/5104260241687538
750/6304260241687545
750/5004260241687507
750/6204260241687514
750/7004260644770752