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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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Mikrobac — 9 UDI-DI variants, MDR (BODE Chemie GmbH)

MD Atlas
BODE Chemie GmbH

Data from EUDAMED, last updated May 23, 2026

Mikrobac

40316783778MJ

9 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: BODE Chemie GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40316783778MJ
Device name: Mikrobac
Device model: 3778
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: BODE Chemie GmbH
SRN: DE-MF-000005851
Country: Germany
Email: regulatoryaffairs@bode-chemie.de

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HF3QMDV8P2AW07THCK83J8H5

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

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97539804031678038053
97539704031678038039
97539504031678036950
98180904031678082674
98168804031678082704
98180804031678082643
98133904031678063918
98138704031678065202