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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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Bima basic recond and Bima basic… — 1 UDI-DI variant, MDR

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

Data from EUDAMED, last updated May 30, 2026

Bima basic recond and Bima basic recond child

7340047310-SERIESW4

1 UDI-DI variant

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

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 7340047310-SERIESW4
Device name: Bima basic recond and Bima basic recond child
Device model: 10-Series and C10-Series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 10, 2025

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

1 UDI-DI variant

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Applied filters

basicUdiUlid01KC4R9NFPGMX9PGAYYWB711S1

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

10-3535-K07340047300804