EUDAMED last updated this device on May 27, 2026

MANY

36640435BE

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LENTILLES
UDI-DI code: 13664043001178
Reference / catalog number: MANY

MANY is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by LENTILLES. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 27, 2026

MANY

36640435BE

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LENTILLES
UDI-DI code: 13664043001178
Reference / catalog number: MANY

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 13664043001178
Basic UDI-DI: 36640435BE
Reference / catalog number: MANY
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: PAUNELENS 3R Toric DK High
Additional information URL: https://www.lcs.guide/fr/notices-lentilles-de-contact/
Clinical sizes: 7.5–11 MU50
10.4–12 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)13664043001178

UDI-PI DataMatrix

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

EMDN nomenclature code(s)

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

Q02100402CONTACT LENSES - NON HYDROGEL

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.

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

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in France; available across 4 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Belgium		Still on market
Luxembourg		Still on market
Romania		Still on market

Device identification

Trade name: not provided
UDI-DI code: 13664043001178
Basic UDI-DI: 36640435BE
Reference / catalog number: MANY
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: PAUNELENS 3R Toric DK High
Additional information URL: https://www.lcs.guide/fr/notices-lentilles-de-contact/
Clinical sizes: 7.5–11 MU50
10.4–12 MU50

Manufacturer information

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)13664043001178

UDI-PI DataMatrix

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

EMDN nomenclature code(s)

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

Q02100402CONTACT LENSES - NON HYDROGEL

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.

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

Certificates

Certificate health across this manufacturer's portfolio.

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

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

All products by LENTILLES

Market distribution

Primary placement in France; available across 4 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Belgium		Still on market
Luxembourg		Still on market
Romania		Still on market

MANY

MANY

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Related devices