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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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TImask Dispositivo medico mascherine… — 84 UDI-DI variants, MDR

MD Atlas
TiMask Suisse Sagl

Data from EUDAMED, last updated May 23, 2026

TImask Dispositivo medico mascherine chirurgiche Tipo IIR

7649989889003P7

84 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: TiMask Suisse Sagl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649989889003P7
Device name: TImask Dispositivo medico mascherine chirurgiche Tipo IIR
Device model: Mascherine chirurgiche
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: TiMask Suisse Sagl
SRN: CH-MF-000025278
Country: Switzerland
Email: commerciale@timask.ch
Phone: +41 79 213 82 95

Authorised representative

Name: UKALIA Limited
SRN: XI-AR-000024526
Country: Northern Ireland
Phone: +44 7497495840

Variants by status

UDI-DI variants

84 UDI-DI variants

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Export results

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basicUdiUlid01G7SJ0EHM8GVVSZX5X953V4D1

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

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