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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

Construction tape CDT — Class I MDR by Eurotape B.V.

MD Atlas
Eurotape B.V.

EUDAMED last updated this device on Feb 13, 2024

Construction tape CDT

871992590CDTU3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Eurotape B.V.
UDI-DI code: 08719925907357
Reference / catalog number: CDT.025200.0F

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View device family (Basic UDI)

Manufacturer information

Organization name: Eurotape B.V.
SRN: NL-MF-000001956
Manufacturer status: Active

Related devices

Construction Tape CDT871992590CDTU3On the market Construction Tape CDT871992590CDTU3On the market Construction Tape CDT871992590CDTU3On the market Construction Tape CDT871992590CDTU3On the market Construction Tape CDT871992590CDTU3On the market

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.

CW009
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: Construction tape CDT
UDI-DI code: 08719925907357
Basic UDI-DI: 871992590CDTU3
Reference / catalog number: CDT.025200.0F
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: —
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

EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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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