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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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Hypomer Baby 100 — 1 UDI-DI variant, MDR (NEOMEDIS)

MD Atlas
NEOMEDIS

Data from EUDAMED, last updated May 19, 2026

Hypomer Baby 100

3760436853760426850005H5

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: NEOMEDIS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3760436853760426850005H5
Device name: Hypomer Baby 100
Device model: ZLAK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEOMEDIS
SRN: FR-MF-000004432
Country: France
Email: info@neomedis.com
Phone: +33 142 888 261

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JWXS6TX6ENCAW73V6AM0Y6E4

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

Hypomer Baby 10003760426850005