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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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Organization name
UDI-DI code
Reference / catalog number

DOUGEL 55 — Class IIa MDR by LENTILLES

MD Atlas
LENTILLES

EUDAMED last updated this device on Mar 4, 2026

DOUGEL 55

36640434BC

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LENTILLES
UDI-DI code: 13664043000652
Reference / catalog number: DOUGEL 55

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View device family (Basic UDI)

Manufacturer information

Organization name: LENTILLES
SRN: FR-MF-000006721
Manufacturer status: Active

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.

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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: 13664043000652
Basic UDI-DI: 36640434BC
Reference / catalog number: DOUGEL 55
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: DOUGEL Spheric H50
Additional information URL: https://www.lcs.guide/fr/notices-lentilles-de-contact/
Clinical sizes: 7.1–9.8 MU50
12.5–16 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)13664043000652

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q0210040102CONTACT LENSES - HYDROGEL, REUSABLE

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

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Certificates

Certificate health across this manufacturer's portfolio.

FR26/0000004Issued
Quality assuranceNotified body: 1639Expiry: Jan 13, 2031