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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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Pacifier for premature babies — 2 UDI-DI variants, MDR

MD Atlas
BELGIAN DIAGNOSTIC COMPANY

Data from EUDAMED, last updated May 23, 2026

Pacifier for premature babies

5414456HPF3714xGT5

2 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: BELGIAN DIAGNOSTIC COMPANY

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5414456HPF3714xGT5
Device name: Pacifier for premature babies
Device model: HPF37140G
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: BELGIAN DIAGNOSTIC COMPANY
SRN: BE-MF-000004224
Country: Belgium
Email: InfoBeldico@beldico.be

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KR3DTYQQ6XZS1WYH8K2H0ECA

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

HPF37140G15414456381408
HPF37141G15414456381415