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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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MOWOOT — 16 UDI-DI variants, MDR (USMIMA, S.L.)

MD Atlas
USMIMA, S.L.

Data from EUDAMED, last updated May 23, 2026

MOWOOT

8437016001MOWOOTII7E

16 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: USMIMA, S.L.

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 8437016001MOWOOTII7E
Device name: MOWOOT
Device model: MOWOOT II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: USMIMA, S.L.
SRN: ES-MF-000000232
Country: Spain
Email: markus.wilhelms@mowoot.com
Phone: (+34) 93 510 66 53

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GZXNNED1RTFP8BCMBERWSD8Y

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

MW2-D0108437016001004
MW2-B0308437016001035
MW2-B0208437016001028
MW2-B0108437016001011
MW2-B0408437016001042
MW2-PS108437016001066
MW3-D0108437016001141
MW3-B0308437016001196
MW3-B0208437016001189
MW3-B0108437016001172
Mw3-B0408437016001202
MW3-PS108437016001158
MW3-B03-Starter08437016001271
MW3-B02-Starter08437016001264
MW3-B01-Starter08437016001257
MW3-B04-Starter08437016001288