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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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HITECH — 6 UDI-DI variants, MDR (INDUSTRIAS HIDRÁULICAS PARDO SL)

MD Atlas
INDUSTRIAS HIDRÁULICAS PARDO SL

Data from EUDAMED, last updated May 23, 2026

HITECH

8431212HITECHQD

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: INDUSTRIAS HIDRÁULICAS PARDO SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431212HITECHQD
Device name: HITECH
Device model: SC80120
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 16, 2024

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

6 UDI-DI variants

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Applied filters

basicUdiUlid01HM8YP4VDANT80HJMH2S1BDZV

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

SC801200000000208431212214350
SC801200000001108431212220795
SC801200000000708431212219409
SC801200000000808431212219591
SC801200000000108431212214107
SC801600000002008431212276952