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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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Healsea Babykids — 4 UDI-DI variants, MDR (Lallemand Pharma)

MD Atlas
Lallemand Pharma

Data from EUDAMED, last updated May 23, 2026

Healsea Babykids

76401497214RR

4 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: Lallemand Pharma

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 76401497214RR
Device name: Healsea Babykids
Device model: Nasal Pump Spray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: Lallemand Pharma
SRN: CH-MF-000036587
Country: Switzerland
Email: officelp@lallemand.com

Authorised representative

Name: ASPE CONSEIL
SRN: FR-AR-000016220
Country: France
Phone: + 33 5 61 23 93 49

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K60MS0B3CY5SKT54XX01JTM2

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

Azéol DM Rhume - Rhinite enfant07640149724301
Healsea Babykids07640149724288
75014DJNP07640149724363
75014DJND07640149724295