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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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CareMin650 ™ Oral Sleeve — 2 UDI-DI variants, MDR (NEOMEDLIGHT)

MD Atlas
NEOMEDLIGHT

Data from EUDAMED, last updated May 19, 2026

CareMin650 ™ Oral Sleeve

376001257CM650Sleeve7A

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: NEOMEDLIGHT

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 376001257CM650Sleeve7A
Device name: CareMin650 ™ Oral Sleeve
Device model: CM211
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: NEOMEDLIGHT
SRN: FR-MF-000004044
Country: France
Email: contact@neomedlight.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQSP9A69XAK4WEF1JWHBD7P8

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

CareMin650 ™ Derma Sleeve03760012570010
CareMin650 ™ Oral Sleeve03760012570034