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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

7007400000 — Class I MDR by Select Sport A/S

MD Atlas
Select Sport A/S

EUDAMED last updated this device on Jan 30, 2024

7007400000

5703543U1006LC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Select Sport A/S
UDI-DI code: 05703543174560
Reference / catalog number: 7007400000

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View device family (Basic UDI)

Manufacturer information

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

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: 05703543174560
Basic UDI-DI: 5703543U1006LC
Reference / catalog number: 7007400000
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: The Profcare Foam tape is intended to be used as a protective layer between skin and friction, which enables tape-removal to be painless and prevents rubbing and irritation from external sources. It is for direct use on (unbroken)skin only - Duration of use should not exceed 3-4 hours Component 80% and 20%
Additional information URL: https://dk.select-sport.com/products/macure-skumtape-720059?_pos=2&_sid=23e4195e2&_ss=r
Clinical sizes: 5 MU10
3 MU36

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05703543174560

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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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