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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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bess|folio restricted — 15 UDI-DI variants, MDR (bess pro gmbh)

MD Atlas
bess pro gmbh

Data from EUDAMED, last updated May 30, 2026

bess|folio restricted

4063106FOLRESNK

15 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: bess pro gmbh

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4063106FOLRESNK
Device name: bess|folio restricted
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: bess pro gmbh
SRN: DE-MF-000006209
Country: Germany
Email: vigilance@besspro.eu
Phone: +49 30 816 909 0

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KSQ5T5B6MEH527NHX19570Q5

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

BM 20 210014063106100152
BM 20 205014063106100145
BM 20 100214063106100183
BM 20 810014063106101609
BM 99 001014063106101692
BM 20 201114063106100114
BM 20 201214063106100121
BM 20 100014063106100169
BM 20 100114063106100176
BM 99 007314063106101654
BM 99 000614063106101715
BM 20 202014063106100138
BM 20 805014063106101593
BM 20 815014063106101616
BM 20 201014063106100107