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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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restifem — 6 UDI-DI variants, MDR (VIOMED Vertriebs GmbH)

MD Atlas
VIOMED Vertriebs GmbH

Data from EUDAMED, last updated May 23, 2026

restifem

PP07643RESTIFEM02

6 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: VIOMED Vertriebs GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP07643RESTIFEM02
Device name: restifem
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: VIOMED Vertriebs GmbH
SRN: DE-MF-000043019
Country: Germany
Email: info@viomed.de
Phone: +493382704280

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KG48EXHBC24RTEA2B18ACEPZ

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

restifem Medium111290223958
restifem pro Large111946619089
restifem pro Medium111946622139
restifem pro Small111946620910
restifem Set111539361469
restifem Small111290222268