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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

20-20TUB — IVDD — General IVDD by Salofa Oy

MD Atlas
Salofa Oy

EUDAMED last updated this device on Aug 28, 2022

20-20TUB

B-FIMF168232020TUBZB

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Salofa Oy
UDI-DI code: D-FIMF168232020TUBZB
Reference / catalog number: 20-20TUB

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Manufacturer information

Organization name: Salofa Oy
SRN: FI-MF-000016823
Manufacturer status: Active

Market distribution

Primary placement in Sweden; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: D-FIMF168232020TUBZB
Basic UDI-DI: B-FIMF168232020TUBZB
Reference / catalog number: 20-20TUB
Issuing entity: EUDAMED

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: Sample tube for rapid test for the detection of fecal occult blood
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0102160203FECAL OCCULT BLOOD - RT & POC

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
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Manufacturing date
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Software identification

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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.