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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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Laerdal Face Shield — 39 UDI-DI variants, MDR (Laerdal Medical AS)

MD Atlas
Laerdal Medical AS

Data from EUDAMED, last updated May 30, 2026

Laerdal Face Shield

0704543209941SW

39 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: Laerdal Medical AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0704543209941SW
Device name: Laerdal Face Shield
Device model: Laerdal Face Shield
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Laerdal Medical AS
SRN: NO-MF-000000012
Country: Norway
Email: PRRC@laerdal.com
Phone: +47 51511700

Variants by status

UDI-DI variants

39 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GG4AEXHETA5RXQ90PKQWQCYK

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

Laerdal Face Shield07045430079304
Laerdal Face Shield07045430079267
Laerdal Face Shield07045430079274
4600000207045430040359
Laerdal Face Shield07045430040502
46000293 07045432117004
4600021107045432116960
4600020407045432116922
46000201 07045432116786
4600020707045432116946
4600021007045432116953
46020507045432116984
4600022907045432116977
4600020207045432116915

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