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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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Furine plus — 12 UDI-DI variants, MDR (Furine ApS)

MD Atlas
Furine ApS

Data from EUDAMED, last updated May 31, 2026

Furine plus

57400089B06XX222U

12 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: Furine ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57400089B06XX222U
Device name: Furine plus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: Furine ApS
SRN: DK-MF-000001231
Country: Denmark
Email: btn@furine.com
Phone: +4529709421

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01FS26CT7T3KB374H5836YA6N1

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

B06ES2205740008901293
B06UK2205740008900975
B06FR2205740008901378
B06IT2205740008901415
B06NL2205740008901491
B06FI2205740008901330
B06PT2205740008901576
B06DE2205740008901217
B06EL2205740008901255
B06DK2205740008900937
B06BM2205740008901132
B06SE2205740008901613