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EUDAMED last updated this device on Sep 18, 2023
B-05903949820584Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →The phototherapy lamp FOTOVITA FV 10S is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by ULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →05903949820584Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →B-05903949820584FV 10SUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →(01)05903949820584
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12040202PHOTOTHERAPY EQUIPMENT5 warnings recorded — scroll inside the panel to see all entries.
CW010CW027CW259CW276CW277Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Still on market |
PL-MF-000002803No 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.TNP/MDD/0241/828/20185903949821000000DICO3ZOn the marketDigital and analogue medical images viewing station type DiCO 1M/1B5903949821000000DICO3ZOn the marketDigital and analogue medical images viewing station type DiCO 1M/2B5903949821000000DICO3ZOn the marketDigital and analogue medical images viewing station type DiCO 2M5903949821000000DICO3ZOn the marketDigital and analogue medical images viewing station type DiCO 2M/1B5903949821000000DICO3ZOn the market