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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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Kanmed BB-CORD — 4 UDI-DI variants, MDR (Kanmed AB)

MD Atlas
Kanmed AB

Data from EUDAMED, last updated May 31, 2026

Kanmed BB-CORD

73500451230311313WP

4 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: Kanmed AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73500451230311313WP
Device name: Kanmed BB-CORD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Kanmed AB
SRN: SE-MF-000001839
Country: Sweden
Email: qara@kanmed.se
Phone: +46 8 564 80 630

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KSSGSQX7HQF9B7XFGQ2CBKW0

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

BB60007350045121905
BBC12507350045122063
BBC12007350045122056
BBC-2007350045121912