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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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73400473(C)10-SERIESTR — 132 UDI-DI variants, MDR

MD Atlas
B.I.M.A. PLASTTEKNIK AB

Data from EUDAMED, last updated May 30, 2026

73400473(C)10-SERIESTR

73400473(C)10-SERIESTR

132 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: B.I.M.A. PLASTTEKNIK AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73400473(C)10-SERIESTR
Device name: —
Device model: 73400473(C)10-SERIESTR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: B.I.M.A. PLASTTEKNIK AB
SRN: SE-MF-000001678
Country: Sweden
Email: info@bimaplastteknik.se
Phone: +4634041950

Variants by status

UDI-DI variants

132 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSF9W6MRENFR93HZZK33N3CG

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

10-5550-P07340047301450
10-3535-P07340047300811
10-3745-K07340047300866
10-4738-K07340047347373
10-3738-K07340047347298
10-4035-P07340047339880
10-4540-K07340047301061

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