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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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Elastic tubular bandage, unbleached… — 8 UDI-DI variants, MDR

MD Atlas
Mediplast AB

Data from EUDAMED, last updated May 31, 2026

Elastic tubular bandage, unbleached cotton

73955026107116BN6

8 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: Mediplast AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73955026107116BN6
Device name: Elastic tubular bandage, unbleached cotton
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mediplast AB
SRN: SE-MF-000000885
Country: Sweden
Email: info.se@mediplast.com
Phone: +46406712300

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KR0K7XG0W6JE1BJE2V1V1PW7

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

605072107395502030772
605072507395502030819
605072607395502030826
605072307395502030796
605073007395502065224
605072407395502030802
605072707395502030833
605072207395502030789