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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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Oral sprays — 8 UDI-DI variants, MDR (Dr. Müller Pharma s.r.o.)

MD Atlas
Dr. Müller Pharma s.r.o.

Data from EUDAMED, last updated May 23, 2026

Oral sprays

85956104PSHW

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Dr. Müller Pharma s.r.o.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2023-MDR/QS-035/B
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Mar 23, 2026 → Oct 20, 2028

Identity & classification

Basic UDI-DI: 85956104PSHW
Device name: Oral sprays
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 12, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01HRS65SY8BKR1F1J5GBTEBYK2

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

PC8903_00208595610406523
PC8901_00308595610406516
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PC8903_00108595610405632
PC8902_00108595610405649
PC8901_00108595610405625
PC8901_00808595610407513
Tussipress oral spray with iceland moss08595610407186