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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

7007305024 — Class I MDR by Select Sport A/S

MD Atlas
Select Sport A/S

EUDAMED last updated this device on Jan 24, 2024

7007305024

5703543U1005LA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Select Sport A/S
UDI-DI code: 05703543202140
Reference / catalog number: 7007305024

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View device family (Basic UDI)

Manufacturer information

Organization name: Select Sport A/S
SRN: DK-MF-000025005
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 1 country total.

Placed on the market in Denmark; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05703543202140
Basic UDI-DI: 5703543U1005LA
Reference / catalog number: 7007305024
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: 24
Additional product description: The Profcare Stretch Tape is intended to be used to support bodyparts within sport active/athletes - and to provide the best possible pre-conditions for movement. It's for direct use on (unbroken)skin only.
Additional information URL: https://dk.select-sport.com/products/stretch-tape-720060?_pos=4&_psq=Stretch&_ss=e&_v=1.0
Clinical sizes: 6.9 MU36
5 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05703543202140

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

M050299PLASTERS FOR EXTENSIVE AREAS - 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

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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.