Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

STAR 4013664043000690
TRABECULENS13664043000430
UM513664043000560
UM513664043000546
UM513664043000553
UM513664043000577
UM513664043000584

1 2 3