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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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Samui® — 2 UDI-DI variants, IVDR (pfm medical gmbh)

MD Atlas
pfm medical gmbh

Data from EUDAMED, last updated May 23, 2026

Samui®

4042301W0202BCTQ

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: pfm medical gmbh

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4042301W0202BCTQ
Device name: Samui®
Device model: Cooling Plate
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: pfm medical gmbh
SRN: DE-MF-000039552
Country: Germany
Email: info@pfmmedical.com
Phone: +49 2236 9641-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KNS20BHHB7JT4HGJSPRVC28D

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

70071004042301218162
70070004042301218155