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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

RGP — Class IIa MDD by CONÓPTICA, S.L.

MD Atlas
CONÓPTICA, S.L.

EUDAMED last updated this device on May 15, 2026

RGP

B-08437022752563

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: CONÓPTICA, S.L.
UDI-DI code: 08437022752563
Reference / catalog number: RGP

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Manufacturer information

Organization name: CONÓPTICA, S.L.
SRN: ES-MF-000040465
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Apr 23, 2004	Dec 31, 2028

Device identification

Trade name: not provided
UDI-DI code: 08437022752563
Basic UDI-DI: B-08437022752563
Reference / catalog number: RGP
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5–10 MU50
7–12.2 MU50
-35–35 MU104

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

Related devices

RGPB-08437022752549On the market RGPB-08437022752600On the market RGPB-08437022752617On the market RGPB-08437022752587On the market RGPB-08437022752624On 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.