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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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FACEPLATES — 3 UDI-DI variants, MDR (WSAUD A/S)

MD Atlas
WSAUD A/S

Data from EUDAMED, last updated May 31, 2026

FACEPLATES

5714880-WSA-20-20-ZJ

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: WSAUD A/S

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5714880-WSA-20-20-ZJ
Device name: —
Device model: FACEPLATES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: WSAUD A/S
SRN: DK-MF-000015974
Country: Denmark
Email: katarzyna.bobrow@wsa.com
Phone: +45 44 35 56 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JZQPXHD6CE54CCKV9MVD9E43

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

C_ITE CIC VOLTA C T05714880184266
C_ITE CIC VOLTA C T505714880184259
C_ITE ITC VOLTA C05714880184273