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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

HK019X050 — IVDD — General IVDD by Hyris Srl

MD Atlas
Hyris Srl

EUDAMED last updated this device on May 29, 2023

HK019X050

B-80575074301460

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Hyris Srl
UDI-DI code: 80575074301460
Reference / catalog number: HK019X050

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View device family (Basic UDI)

Manufacturer information

Organization name: Hyris Srl
SRN: IT-MF-000031635
Manufacturer status: Active

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bCUBE 2.0805750743BCUBEA9On the market H0001805750743H0001XVOn the market HK032X300B-80575074301156On the market HK032X260B-80575074301088On the market HK032X130B-80575074300920On 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 Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 80575074301460
Basic UDI-DI: B-80575074301460
Reference / catalog number: HK019X050
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: HK019X050
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.

W01030699LYMPHOKINES /IMMUNMODULATORS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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