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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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Emovo Wear — 6 UDI-DI variants, MDR (Emovo Care)

MD Atlas
Emovo Care

Data from EUDAMED, last updated May 23, 2026

Emovo Wear

7649995625EW1QG

6 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: Emovo Care

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649995625EW1QG
Device name: Emovo Wear
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: Emovo Care
SRN: CH-MF-000049487
Country: Switzerland
Email: hello@emovocare.com
Phone: +41215881875

Authorised representative

Name: Donawa Lifescience Consulting Srl
SRN: IT-AR-000007785
Country: Italy
Phone: +39 06 578 2665

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KN71BDKHEXPTM4N89VGDVXJV

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

EW1-RM107649995625053
EW1-LL107649995625091
EW1-LS107649995625077
EW1-RL107649995625060
EW1-RS107649995625046
EW1-LM107649995625084