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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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Rectal suppositories — 3 UDI-DI variants, MDR (VH Pharma a.s.)

MD Atlas
VH Pharma a.s.

Data from EUDAMED, last updated May 23, 2026

Rectal suppositories

859417749HEMAGELPROCTOTN

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: VH Pharma a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859417749HEMAGELPROCTOTN
Device name: Rectal suppositories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: VH Pharma a.s.
SRN: CZ-MF-000005951
Country: Czechia
Email: vhpharma@vhpharma.cz
Phone: +420 377 429 448

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRDDJCTQM773W69M2ZTH7JAT

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

HP-508594177490310
HP-1508594177490334
HP-1008594177490327