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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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Idracare — 3 UDI-DI variants, MDR (Procare Health Iberia SL)

MD Atlas
Procare Health Iberia SL

Data from EUDAMED, last updated May 23, 2026

Idracare

8437018976IDRF2

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: Procare Health Iberia SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437018976IDRF2
Device name: Idracare
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 21, 2022

Manufacturer & authorised representative

Manufacturer

Name: Procare Health Iberia SL
SRN: ES-MF-000001950
Country: Spain
Email: info@procarehealth.com
Phone: +34 936 455 441

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FYPMB4Z34FPTE1H8K9X0K1C8

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

Idracare Vaginal Gel08437018976416
Idracare Vaginal Gel08437018976409
Idracare Vaginal Gel08436620080993