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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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STERILE SOFT CONTACT LENS — 57 UDI-DI variants, MDR (LENTILLES)

MD Atlas
LENTILLES

Data from EUDAMED, last updated May 19, 2026

STERILE SOFT CONTACT LENS

36640434BC

57 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: LENTILLES

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: FR26/0000004
Type: refdata.certificate-mdr-type.quality-assurance
Notified body: SGS Belgium NV (1639)
Validity: Jan 13, 2026 → Jan 13, 2031

Identity & classification

Basic UDI-DI: 36640434BC
Device name: —
Device model: STERILE SOFT CONTACT LENS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.made-to-order
Version date: Feb 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: LENTILLES
SRN: FR-MF-000006721
Country: France
Email: info@laboratoire-lcs.com
Phone: +33231866656

Variants by status

UDI-DI variants

57 UDI-DI variants

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Applied filters

basicUdiUlid01K1Z9PYE4JEJD2XTXC18TK6RR

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

No registered UDI-DI variants for this device family.