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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

CANNASEN® Pain Patch [EN] — Class I MDD by Cannordic A/S

MD Atlas
Cannordic A/S

EUDAMED last updated this device on Jan 14, 2025

CANNASEN® Pain Patch [EN]

B-05744000130217

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Cannordic A/S
UDI-DI code: 05744000130217
Reference / catalog number: 87652A

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View device family (Basic UDI)

Manufacturer information

Organization name: Cannordic A/S
SRN: DK-MF-000003852
Manufacturer status: Active

Critical warnings

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

CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Denmark; available across 2 countries total.

Country	On market since	Until
DenmarkPrimary placement		Still on market
Croatia	Jan 1, 2025	Still on market

Device identification

Trade name: CANNASEN® Pain Patch [EN]
UDI-DI code: 05744000130217
Basic UDI-DI: B-05744000130217
Reference / catalog number: 87652A
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: "CANNASEN® Pain Patch is used for the relief of muscle/joint pain (such as arthritis, back pain, sprains, sports injuries). CANNASEN® Pain Patch provides a long lasting pain relief" [EN]
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

UDI-DI DataMatrix

Encoded

(01)05744000130217

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EMDN nomenclature code(s)

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

M9001CRYOTHERAPY AND THERMOTHERAPY DEVICES

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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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.