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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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BODE X-Wipes — 2 UDI-DI variants, MDR (BODE Chemie GmbH)

MD Atlas
BODE Chemie GmbH

Data from EUDAMED, last updated May 23, 2026

BODE X-Wipes

40316783775MC

2 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: BODE Chemie GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40316783775MC
Device name: BODE X-Wipes
Device model: 3775
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 31, 2022

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

2 UDI-DI variants

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Applied filters

basicUdiUlid01GBSRKV0MNJR1ZJ6TT5SNZV2C

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

98147904031678070923
98194504031678085828