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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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Light Protective Cover — 4 UDI-DI variants, MDR (Baxter Healthcare SA)

MD Atlas
Baxter Healthcare SA

Data from EUDAMED, last updated May 23, 2026

Light Protective Cover

00854120000000000000103HV

4 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: Baxter Healthcare SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 00854120000000000000103HV
Device name: Light Protective Cover
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Baxter Healthcare SA
SRN: CH-MF-000026124
Country: Switzerland
Email: simone_diorio@baxter.com
Phone: +41 (79) 4413671

Authorised representative

Name: Baxter Deutschland GmbH
SRN: DE-AR-000010308
Country: Germany
Phone: +49 89 317010

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KGMFZ4HVGTEM1R8DCQ5NF6E3

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

Baxter00085412679211
Baxter00085412679228
Baxter00085412679235
Baxter00085412679259