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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

Riga — Class I MDR by MelaMedic ApS

MD Atlas
MelaMedic ApS

EUDAMED last updated this device on Apr 29, 2026

Riga

5711669MMSG01Y3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MelaMedic ApS
UDI-DI code: 05711669000786
Reference / catalog number: MM-078

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Manufacturer information

Organization name: MelaMedic ApS
SRN: DK-MF-000042515
Manufacturer status: Active

Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: Riga
UDI-DI code: 05711669000786
Basic UDI-DI: 5711669MMSG01Y3
Reference / catalog number: MM-078
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Specifications Recommended users: 12+ For use with prescription- or reading glasses Lenses: Polycarbonate with orange filter UV-530 - Scratch-resistant surface Frame material: Metal and rubber Frame colour: Dark gray Glasses width: 131 mm Glasses height: 46 mm Glasses bridge: 12 mm Weight: 9 grams Glasses case: Polypropylene (PP) - Solid-dyed light gray Cleaning cloth: Grey textile (80% polyester / 20% polyamide) Manual: Danish, Dutch, English, Finnish, French, German, Icelandic, Italian, Norwegian, Portuguese, Spanish and Swedish Registered as a medical device according to EU directive 2017/745/EU.
Additional information URL: https://melamedic.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q0210030102READY TO WEAR PLASTIC SPECTACLES WITH ORGANIC LENSES

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

Tallinn5711669MMSG01Y3On the market Vilnius5711669MMSG01Y3On 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.