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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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VARIAX 2 WRIST FUSION - PLATE -… — 3 UDI-DI variants, MDR

MD Atlas
Stryker GmbH

Data from EUDAMED, last updated May 23, 2026

VARIAX 2 WRIST FUSION - PLATE - TITANIUM - CLASS IIB - NON STERILE

08858251003315SM

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Stryker GmbH

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 08858251003315SM
Device name: VARIAX 2 WRIST FUSION - PLATE - TITANIUM - CLASS IIB - NON STERILE
Device model: 08858251003315SM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Stryker GmbH
SRN: CH-MF-000009332
Country: Switzerland
Email: RegulatoryAffairsTE@stryker.com
Phone: +41 (0)32 641 6666

Authorised representative

Name: Stryker European Operations Limited
SRN: IE-AR-000000092
Country: Ireland
Phone: +353 (83) 2030261

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2NQJFT6E9WK5TEFZKFSWV1

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

62958907613327131444
62957907613327131567
62959007613327131536