Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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.

Organization name
UDI-DI code
Reference / catalog number

SLEEP&SEE — Class IIa MDR by LABORATOIRE PRECILENS

MD Atlas
LABORATOIRE PRECILENS

EUDAMED last updated this device on May 3, 2026

SLEEP&SEE

3666486Orthokametropie66

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRE PRECILENS
UDI-DI code: 03666486000858
Reference / catalog number: SLEEP&SEE

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?

Manufacturer information

Organization name: LABORATOIRE PRECILENS
SRN: FR-MF-000000913
Manufacturer status: Active

Related devices

Many3666486ScontrolmyopiaSXOn the market Many3666486SametropieCXOn the market AZUR - TE3666486RametropieC2On the market BIB3666486RpresbytieNPOn the market Sphérique - T - TT - NVS - NVST3666486SametropieCXOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW254
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03666486000858
Basic UDI-DI: 3666486Orthokametropie66
Reference / catalog number: SLEEP&SEE
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Lentille de contact d'orthokératologie pour amétropie
Additional information URL: https://www.precilens.com/notices-lentilles.php
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q02100499CONTACT LENSES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification