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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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STERTOUCH PRO — 8 UDI-DI variants, MDR (C. H. Müller Industries GmbH)

MD Atlas
C. H. Müller Industries GmbH

Data from EUDAMED, last updated May 23, 2026

STERTOUCH PRO

426238301STERILFOLIE_01SC

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: C. H. Müller Industries GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426238301STERILFOLIE_01SC
Device name: STERTOUCH PRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: C. H. Müller Industries GmbH
SRN: DE-MF-000027887
Country: Germany
Email: regulatory.affairs@chmueller.com
Phone: +49 3765 3939 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JXHM327V40EMDD3Y9NDJQ2V8

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

FW2628004262383010045
FW2628104262383010380
FW2628704262383010021
FW2628804262383010007
FW2630104262383010328
FW2637404262383010229
FW26375 04262383010243
FW2637604262383010205