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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

8721325502018 — Class I MDR by Govic

MD Atlas
Govic

EUDAMED last updated this device on Apr 3, 2026

8721325502018

872132550zool17E

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Govic
UDI-DI code: 08721325502018
Reference / catalog number: 8721325502018

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View device family (Basic UDI)

Manufacturer information

Organization name: Govic
SRN: NL-MF-000053016
Manufacturer status: Active

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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

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

CW999
Contra-indications: Not suitable for use on open wounds. Warning: People with diabetes or circulatory problems should consult a medical professional before use.

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Market distribution

Primary placement in Belgium; available across 2 countries total.

Country	On market since	Until
BelgiumPrimary placement	Apr 3, 2026	Still on market
Netherlands	Apr 3, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08721325502018
Basic UDI-DI: 872132550zool17E
Reference / catalog number: 8721325502018
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: Orthopedische Inlegzolen voor Boogondersteuning – Comfort en Correctie Speciaal ontworpen om platvoeten, overpronatie en voetpijn te verlichten. Geschikt voor Hielspoor
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)

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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