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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

704_005 — Class IIa MDD by Fysioline Oy

MD Atlas
Fysioline Oy

EUDAMED last updated this device on Dec 7, 2021

704_005

B-06418029704009

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Fysioline Oy
UDI-DI code: 06418029704009
Reference / catalog number: 704_005

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Manufacturer information

Organization name: Fysioline Oy
SRN: FI-MF-000001173
Manufacturer status: Active

Related devices

800_546B-84353737087347JOn the market 800_350B-64129889131687JOn the market 704_001B-06418029707000On the market 704_010B-06418029707017On the market 704_0001B-06418029905994On 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

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

CW057
Helposti syttyvä neste ja höyry.
CW085
Ärsyttää voimakkaasti silmiä.
CW139
Suojaa lämmöltä, kuumilta pinnoilta, kipinöiltä, avotulelta ja muilta sytytyslähteiltä. Tupakointi kielletty.
CW148
Säilytä tiiviisti suljettuna.
CW416
JOS KEMIKAALIA JOUTUU SILMIIN: Huuhdo huolellisesti vedellä usean minuutin ajan.
CW201
Poista mahdolliset piilolinssit, jos sen voi tehdä helposti. Jatka huuhtomista.

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Dec 14, 2007	Still on market

Device identification

Trade name: not provided
UDI-DI code: 06418029704009
Basic UDI-DI: B-06418029704009
Reference / catalog number: 704_005
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Lindrignt denaturerad etanollösning är avsedd för desinfektion av icke-invasiva medicintekniska produkter ock verktyg samt för desinficering av hud innan behandling. Desinfektionstid för alkoholen är dess torkningstid.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5 MU02

EMDN nomenclature code(s)

D0701ETHANOL FOR THE DISINFECTION OF MEDICAL 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification