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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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IceCap 2 — 9 UDI-DI variants, MDR (BIOSERENITY MEDICAL DEVICES GROUP)

MD Atlas
BIOSERENITY MEDICAL DEVICES GROUP

Data from EUDAMED, last updated May 19, 2026

IceCap 2

361522WEMUelectrodsFY

9 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: BIOSERENITY MEDICAL DEVICES GROUP

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 361522WEMUelectrodsFY
Device name: IceCap 2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: BIOSERENITY MEDICAL DEVICES GROUP
SRN: FR-MF-000039391
Country: France
Email: pierre.emerich@bioserenity.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01JJ6KS2MAZ90XRVJNK29CWV76

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

Neuronaute® Touchproof Adapter03615220003846
Neuronaute® IceAdapter03615220003624
Neuronaute® IceCap 203615220003617
Neuronaute® IceCap 203615220004331
Neuronaute® IceCap 2 Small03615220004355
Neuronaute® IceCap 2 Small03615220003792
Neuronaute® IceCap Neonate (M)03615220003952
Neuronaute® IceCap Neonate (S)03615220003969
Neuronaute®IceCap Neonate (XS)03615220003976