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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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ZCP — 2 UDI-DI variants, MDR (Valley Electronics AG)

MD Atlas
Valley Electronics AG

Data from EUDAMED, last updated May 23, 2026

ZCP

7629999ZCPRZ

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: Valley Electronics AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7629999ZCPRZ
Device name: ZCP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: Valley Electronics AG
SRN: CH-MF-000014362
Country: Switzerland
Email: info@valley-electronics.ch
Phone: +41 44 577 68 69

Authorised representative

Name: M.I.S.S. GmbH
SRN: DE-AR-000011822
Country: Germany
Phone: +49 8841 4854166

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JA7NVR716CP2NE1QG81YXABT

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

Daysy07629999054073
Lady-Comp07629999894334