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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

7008940111 — Class I MDR by Select Sport A/S

MD Atlas
Select Sport A/S

EUDAMED last updated this device on Jan 29, 2024

7008940111

5703543U1011L5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Select Sport A/S
UDI-DI code: 05703543236138
Reference / catalog number: 7008940111

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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: 05703543236138
Basic UDI-DI: 5703543U1011L5
Reference / catalog number: 7008940111
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: 2
Additional product description: The Profcare Pro Strap Tape is intended to be used to support body parts in sports athletes and active human beings. It's intended to prevent injury or reinjury by stabilizing body parts and guiding correct movement within a degree of ROM. To prevent and treat injuries by immobilization It is for direct use on (unbroken)skin only. Component: 50% fabric, 50% adhesive
Additional information URL: https://dk.select-sport.com/products/pro-strap-sportstape-2-pak-720114?_pos=3&_sid=a841f8411&_ss=r
Clinical sizes: 4 MU10
10 MU36

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05703543236138

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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.