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EUDAMED last updated this device on Mar 10, 2026
37014371BU684X10XCL1SSAROMAPOUX is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by TAG LIFECARE. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03701437100055BU684-103 packaging levels registered — each level carries its own UDI-DI.
03701437100055× 1 unitBase unit03701437120053× 12 units03701437110054× 2 units03701437130052× 9 units(01)03701437100055
European Medical Device Nomenclature — the EU product classification assigned to this device.
V901001LICE ELIMINATION MECHANICAL DEVICES7 warnings recorded — scroll inside the panel to see all entries.
Do not apply on damaged and irrited skin. Repeated use: Do not apply for children under 3 years old. Do not leave on for more than 5 minutes. Do not apply for children under 6 months old. Do not use in combination with any other scalp treatment without medical advice. Do not use on damaged scalps (psoriasis, lichen, seborrhoeic dermatitis, etc.) without medical advice.
Contact a doctor showing the packaging of the product.
Rinse cautiously with water for several minutes.
Primary placement in Belgium; available across 1 country total.
Placed on the market in Belgium; per-country availability dates not published.
FR-MF-000000300The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
In this case, stop the treatment, rinse, consult a doctor if persists.
Do not use in case of known allergy to any of the ingredients.
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.
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 →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 →Basic 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 →UDI 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 →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 →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.No certificate specifically references this device's Basic UDI-DI.