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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

FRIGOFAST GHIACCIO 200 ML EN/AR — Class IIa MDR by TOSVAR srl

MD Atlas
TOSVAR srl

EUDAMED last updated this device on Jan 26, 2023

FRIGOFAST GHIACCIO 200 ML EN/AR

8028356SS15001ALM

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TOSVAR srl
UDI-DI code: 08028356000866
Reference / catalog number: SS15001A

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View device family (Basic UDI)

Manufacturer information

Organization name: TOSVAR srl
SRN: IT-MF-000013303
Manufacturer status: Active

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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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW038
Danger Extremely flammable aerosol. Pressurised container: May burst if heated. Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Do not pierce or burn, even after use. Protect from sunlight. Do not expose to temperatures exceeding 50°C/122°F. Keep out of reach of children Do not spray on an open flame or other ignition source

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	Jun 30, 2004	Still on market
Poland	Jan 1, 2020	Still on market

Device identification

Trade name: FRIGOFAST GHIACCIO 200 ML EN/AR
UDI-DI code: 08028356000866
Basic UDI-DI: 8028356SS15001ALM
Reference / catalog number: SS15001A
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
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.

M9001CRYOTHERAPY AND THERMOTHERAPY DEVICES

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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