EUDAMED last updated this device on May 27, 2026

NORDALYN ACTIVE 500ml

B-06430070090801

On the marketClass I

Applicable legislation: —
Organization name: Viking Lab Oy
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 06430070090801
Reference / catalog number: ND2006

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

NORDALYN ACTIVE 500ml is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Viking Lab Oy. Placed on the EU market in Finland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: NORDALYN ACTIVE 500ml
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 06430070090801
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: B-06430070090801
Reference / catalog number: ND2006
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class I
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: NORDALYN ACTIVE (COLD-HEAT GEL) Pain relief gel is a fast and effective dual acting treatment for repetitive strain injury and sports related pain. Cold reduces swelling, cooling and warming effect releases muscle tension and speeds up recovery in injuries and muscle exertion. INDICATIONS: For the temporary relief of minor aches and pains of muscles and joints. DIRECTION FOR USE: Apply a thin layer to affected area. Repeat as necessary, but not more than 4 times daily. Consult a doctor before use if you are pregnant or nursing or have sensitive skin. Wash hands after use. WARNINGS: For external use only. Do not use on wounds or damaged skin. Do not apply to irritated skin or if excessive irritation develops. Avoid contact with the eyes and mucous membranes. Do not use with other creams, gels, or devices. Do not bandage. Store in a cool and dry place with lid closed tightly. Keep away from excessive heat. Any serious incident that has occurred in relation to the product should be reported to the manufacturer. KEEP OUT OF REACH OF CHILDREN UNDER 12 YEARS OLD
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
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Software identification

UDI-DI DataMatrix

Encoded

(01)06430070090801

EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Critical warnings

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

Caution
For external use only. Do not use on wounds or damaged skin. Do not apply to irritated skin or if excessive irritation develops. Avoid contact with the eyes and mucous membranes. Do not use with other creams, gels, or devices. Do not bandage. Store in a cool and dry place with lid closed tightly. Keep away from excessive heat. Any serious incident that has occurred in relation to the product should be reported to the manufacturer. KEEP OUT OF REACH OF CHILDREN UNDER 12 YEARS OLD

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Apr 10, 2019	Still on market

NORDALYN ACTIVE 500ml

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UDI-DI DataMatrix

EMDN nomenclature code(s)

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UDI-DI DataMatrix

EMDN nomenclature code(s)

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