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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

FT 001 Fevertest — Class I MDD by I.P.S. INTERNATIONAL…

MD Atlas
I.P.S. INTERNATIONAL PRODUCTS e SERVICES Srl

EUDAMED last updated this device on Mar 17, 2025

FT 001 Fevertest

B-08008687000124

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: I.P.S. INTERNATIONAL PRODUCTS e SERVICES Srl
UDI-DI code: 08008687000124
Reference / catalog number: FT 001 Fevertest

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Manufacturer information

Organization name: I.P.S. INTERNATIONAL PRODUCTS e SERVICES Srl
SRN: IT-MF-000029091
Manufacturer status: Active

Related devices

F-TESTB-08008687000117On the market F2B-08008687000087On the market F3B-08008687000094On the market F4B-08008687000100On the market FM 001 48h Fever MonitorB-08008687000131On the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Dec 17, 2014	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08008687000124
Basic UDI-DI: B-08008687000124
Reference / catalog number: FT 001 Fevertest
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Body temperature indicator
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.

V03010199THERMOMETERS - 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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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.