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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

Biostop Shampooing Contrepoux — Class I MDR by TAG LIFECARE

MD Atlas
TAG LIFECARE

EUDAMED last updated this device on Jan 14, 2026

Biostop Shampooing Contrepoux

37014371ONG4X11XCL1Y3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TAG LIFECARE
UDI-DI code: 03701437100307
Reference / catalog number: LIO-SH01

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Manufacturer information

Organization name: TAG LIFECARE
SRN: FR-MF-000000300
Manufacturer status: Active

Critical warnings

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

CW010
Do not apply on damaged and irrited skin. Do not use for children under: 3 years 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.
CW032
EUDAMED did not publish a description for this code.
CW135
EUDAMED did not publish a description for this code.
CW353
Contact a doctor showing the packaging of the product.
CW416
Rinse cautiously with water for several minutes.
CW196
In this case, stop the treatment, rinse, consult a doctor if persists.
CW083
Do not use in case of known allergy to any of the ingredients.

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Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Biostop Shampooing Contrepoux
UDI-DI code: 03701437100307
Basic UDI-DI: 37014371ONG4X11XCL1Y3
Reference / catalog number: LIO-SH01
Issuing entity: GS1

Classification

Risk category: Class I
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.

V901001LICE ELIMINATION MECHANICAL 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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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.