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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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SURFASOFT® monofilament non-adherent… — 3 UDI-DI variants, MDR

MD Atlas
HAROMED B.V.

Data from EUDAMED, last updated May 23, 2026

SURFASOFT® monofilament non-adherent micro-perforated protective contact layer 10 cm x 15 cm

54200791SURFASOFTPS

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: HAROMED B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 54200791SURFASOFTPS
Device name: SURFASOFT® monofilament non-adherent micro-perforated protective contact layer 10 cm x 15 cm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: HAROMED B.V.
SRN: BE-MF-000040766
Country: Belgium
Email: info@haromed.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KM7XB43XZAP6YB7QXNVJ0WFJ

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

1015S05420079100015
5065S05420079100053
2033S05420079100039