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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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PHS — 5 UDI-DI variants, MDR (medica Medizintechnik GmbH)

MD Atlas
medica Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

PHS

4041925PHSBQ

5 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: medica Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4041925PHSBQ
Device name: PHS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: medica Medizintechnik GmbH
SRN: DE-MF-000005058
Country: Germany
Email: info@thera-trainer.com
Phone: +49 7 355 93 14-0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K9W5VB64WGJPH30778N353QR

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

A008-68804041925006360
A008-68704041925006353
A008-68604041925006346
A008-68904041925006377
A008-68504041925006339