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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

KR07-20 — IVDD — General IVDD by FAR Srl

MD Atlas
FAR Srl

EUDAMED last updated this device on May 13, 2026

KR07-20

B-08034063842774

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: FAR Srl
UDI-DI code: 08034063842774
Reference / catalog number: KR07-20

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Manufacturer information

Organization name: FAR Srl
SRN: IT-MF-000041136
Manufacturer status: Active

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW265
EUDAMED did not publish a description for this code.
CW133
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	May 2, 2022	May 13, 2026
EL	Aug 1, 2022	May 13, 2026

Device identification

Trade name: not provided
UDI-DI code: 08034063842774
Basic UDI-DI: B-08034063842774
Reference / catalog number: KR07-20
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: Quantitative determination of 5-Hydroxy-3-Indoleacetic Acid and Serotonin in urine samples. For in vitro diagnostic use only. IVD
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.

W01020390045 HIAA

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

KR12-20B-08034063842798On 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.