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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

4056 — Class I MDR by Hanotex International BV

MD Atlas
Hanotex International BV

EUDAMED last updated this device on Mar 19, 2024

4056

87193263861HITelemetryAU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Hanotex International BV
UDI-DI code: 08719326386195
Reference / catalog number: 4056

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View device family (Basic UDI)

Manufacturer information

Organization name: Hanotex International BV
SRN: NL-MF-000023987
Manufacturer status: Active

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406487193263861HITelemetryAUOn the market 406587193263861HITelemetryAUOn the market 406687193263861HITelemetryAUOn the market 406787193263861HITelemetryAUOn the market 407387193263861HITelemetryAUOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Norway; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08719326386195
Basic UDI-DI: 87193263861HITelemetryAU
Reference / catalog number: 4056
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: 22
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.

Z1399NON-SPECIFIC CONSUMABLES FOR DIAGNOSTIC INSTRUMENTS - 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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