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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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Watherbath Accessories — 3 UDI-DI variants, IVDR (pfm medical gmbh)

MD Atlas
pfm medical gmbh

Data from EUDAMED, last updated May 23, 2026

Watherbath Accessories

4042301W0202BBTN

3 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: 4042301W0202BBTN
Device name: Watherbath Accessories
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 17, 2024

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01HMBSVHP2R0FXA6D8X8S47AX9

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

Cover Waterbath04042301173287
Reflection plate black04042301199911
Reflection Plate Waterbath04042301173270