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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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Sterile Shields — 2 UDI-DI variants, MDR (Toul Meditech AB)

MD Atlas
Toul Meditech AB

Data from EUDAMED, last updated May 30, 2026

Sterile Shields

735010164LAFCU

2 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: Toul Meditech AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735010164LAFCU
Device name: Sterile Shields
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Toul Meditech AB
SRN: SE-MF-000005195
Country: Sweden
Email: info@toulmeditech.com
Phone: +4613215000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSJ6A3GP66B8JJ5FDX9E5NFK

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

LAF-0207350101640012
LAF-02-D07350101640074