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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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G. HELIA/ 100X194 F.I. ABS RHM — 37 UDI-DI variants, MDR

MD Atlas
INDUSTRIAS HIDRÁULICAS PARDO SL

Data from EUDAMED, last updated May 23, 2026

G. HELIA/ 100X194 F.I. ABS RHM

8431212HELIAR7

37 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: INDUSTRIAS HIDRÁULICAS PARDO SL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8431212HELIAR7
Device name: G. HELIA/ 100X194 F.I. ABS RHM
Device model: SG8012310019400
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: INDUSTRIAS HIDRÁULICAS PARDO SL
SRN: ES-MF-000015121
Country: Spain
Email: dalvarez@pardo.es

Variants by status

UDI-DI variants

37 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H6NWPBHJHD21KBXGN4YF9RPA

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

No registered UDI-DI variants for this device family.