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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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ShaverBlades — 177 UDI-DI variants, MDR (DEWIMED Medizintechnik GmbH)

MD Atlas
DEWIMED Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

ShaverBlades

4035282REMAShaverBlades3W

177 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: DEWIMED Medizintechnik GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4035282REMAShaverBlades3W
Device name: ShaverBlades
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: DEWIMED Medizintechnik GmbH
SRN: DE-MF-000011317
Country: Germany
Email: info@dewimed.de
Phone: +49 746292390

Variants by status

UDI-DI variants

177 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQF79DVEJWF16A5PHK3TBF00

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

15-6542004035282353861
15-7632004035282354745

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