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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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Omniplast — 8 UDI-DI variants, MDR (LABORATORIOS HARTMANN S.A.)

MD Atlas
LABORATORIOS HARTMANN S.A.

Data from EUDAMED, last updated May 23, 2026

Omniplast

84105582559QZ

8 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: LABORATORIOS HARTMANN S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84105582559QZ
Device name: Omniplast
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: LABORATORIOS HARTMANN S.A.
SRN: ES-MF-000002991
Country: Spain
Email: LHSA-eudamed@hartmann.info
Phone: +34 626977958

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KRE6JWCYJGWTRRCRDNRTB89J

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

900594208410558002647
900644208410558002616
900578208410558002678
900684208410558002586
900692208410558002500
900690208410558002562
900691208410558002531
900693208410558002470