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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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DermaPlast Compress Gel — 3 UDI-DI variants, MDR (IVF HARTMANN AG)

MD Atlas
IVF HARTMANN AG

Data from EUDAMED, last updated May 23, 2026

DermaPlast Compress Gel

76116001422M4

3 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: IVF HARTMANN AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76116001422M4
Device name: DermaPlast Compress Gel
Device model: 1422
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: IVF HARTMANN AG
SRN: CH-MF-000015962
Country: Switzerland
Email: heinrich.giegrich@hartmann.info
Phone: +41 52 674 35 81

Authorised representative

Name: PAUL HARTMANN AG
SRN: DE-AR-000007519
Country: Germany

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KHB0TNC3XC0Q4NEQ620X6KP7

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

21870007611600953561
21871007611600953578
21872007611600953585