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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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KOMPLET FUTURE MODEL MB — 2 UDI-DI variants, MDR

MD Atlas
INDUSTRIAS HIDRÁULICAS PARDO SL

Data from EUDAMED, last updated May 23, 2026

KOMPLET FUTURE MODEL MB

8431212KOMPLET-FUTURE-29

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: INDUSTRIAS HIDRÁULICAS PARDO SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431212KOMPLET-FUTURE-29
Device name: KOMPLET FUTURE MODEL MB
Device model: SC8018100000020
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 7, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01H77GH1JXEZA41MTVS6YCMMQ1

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

SC801810000002008431212217122
SC801810000002108431212217139