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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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GRW - 100 1" ST — 30 UDI-DI variants, MDR (BEKA-Hospitec GmbH)

MD Atlas
BEKA-Hospitec GmbH

Data from EUDAMED, last updated May 23, 2026

GRW - 100 1" ST

426068189109BZ

30 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: BEKA-Hospitec GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426068189109BZ
Device name: GRW - 100 1" ST
Device model: K109 BEKA Hydrotherapie Produkte und deren Zubehör
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 2024

Manufacturer & authorised representative

Manufacturer

Name: BEKA-Hospitec GmbH
SRN: DE-MF-000013895
Country: Germany
Email: qm@beka-hospitec.de
Phone: +496419222025

Variants by status

UDI-DI variants

30 UDI-DI variants

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Applied filters

basicUdiUlid01HV1A2AC8A0AT8SW2FNBWG31J

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

K109 BEKA Hydrotherapie Produkte und deren Zubehör04260715452945
K109 BEKA Hydrotherapie Produkte und deren Zubehör04260715452969
K109 BEKA Hydrotherapie Produkte und deren Zubehör04260715453119
K109 BEKA Hydrotherapie Produkte und deren Zubehör04260715453126
K109 BEKA Hydrotherapie Produkte und deren Zubehör04260715453133

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