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EUDAMED last updated this device on Jul 1, 2022
3518640000337GPARASIDOSE Producto de tratamiento antipiojos y liendres is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Laboratoires Gilbert. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
FR-MF-000001710(01)03518646043253
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
5 warnings recorded — scroll inside the panel to see all entries.
OTHER
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Romania; available across 1 country total.
Placed on the market in Romania; per-country availability dates not published.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03518646043253Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
3518640000337G604325UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V901001LICE ELIMINATION MECHANICAL DEVICESPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
B-720016NPOn the marketMULTIPHARMA Sérum physiologiqueB-720015NMOn the marketPARASIDOSE Lice and nits care treatment3518640000337GOn the marketPARASIDOSE Producto de tratamiento antipiojos y liendres3518640000337GOn the marketPARASIDOSE Soin traitant anti-poux et lentes3518640000337GOn the marketPARASIDOSE Soin traitant anti-poux et lentes3518640000337GOn the marketNo 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.