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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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Gel pro sonografii Dr. Müller Pharma — 7 UDI-DI variants, MDR

MD Atlas
Dr. Müller Pharma s.r.o.

Data from EUDAMED, last updated May 23, 2026

Gel pro sonografii Dr. Müller Pharma

85956104USG7P

7 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: Dr. Müller Pharma s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85956104USG7P
Device name: Gel pro sonografii Dr. Müller Pharma
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Dr. Müller Pharma s.r.o.
SRN: CZ-MF-000000005
Country: Czechia
Email: info@muller-pharma.cz
Phone: +420 495 809 111

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01J6VGJB9H0P87FSEK2VYGYWWM

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

PC0101_00608595610405700
PC0101_00308595610405441
PC0130_00108595610405458
PC0101_00208595610405434
PC0101_00408595610405465
PC0101_00508595610405540
PC0101_00708595610406141