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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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Zido — 6 UDI-DI variants, MDR (United Care Products B.V.)

MD Atlas
United Care Products B.V.

Data from EUDAMED, last updated May 31, 2026

Zido

872061814319DV

6 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: United Care Products B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 872061814319DV
Device name: Zido
Device model: Zido
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: United Care Products B.V.
SRN: NL-MF-000035901
Country: Netherlands
Email: info@unitedcare.nl
Phone: +31 (0) 50 30 50 900

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K2C79YXB610AEQF4H6MCRFBW

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

1900180008720618143273
1900166008720618143266
1900179008720618143259
1900157008720618143242
1900129008720618143228
1900178008720618143235