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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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ELASTUS® HydroZink — 6 UDI-DI variants, MDR

MD Atlas
Most Active Health Care GmbH

Data from EUDAMED, last updated May 23, 2026

ELASTUS® HydroZink

PP01576MAHCFV000501

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: Most Active Health Care GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP01576MAHCFV000501
Device name: ELASTUS® HydroZink
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Most Active Health Care GmbH
SRN: DE-MF-000013735
Country: Germany
Email: n.staender@most-active.de
Phone: +4915121293510

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GDMTEBVVA1KK9KN4C9YZV8Y3

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

71022111421118966
71021111667866138
71026111421126164
71023111421120326
71024111421122679
71025111421125501