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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

Alhydran Anti Itch Care 59ml — Class I MDR by BAP Medical B.V.

MD Atlas
BAP Medical B.V.

EUDAMED last updated this device on Apr 28, 2026

Alhydran Anti Itch Care 59ml

5425013000116PB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BAP Medical B.V.
UDI-DI code: 05425013009997
Reference / catalog number: 20-31050

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View device family (Basic UDI)

Manufacturer information

Organization name: BAP Medical B.V.
SRN: NL-MF-000002030
Manufacturer status: Active

Related devices

Alhydran 100ml5425013000116PBOn the market Alhydran 15ml5425013000116PBOn the market Alhydran 250ml5425013000116PBOn the market Alhydran 30ml5425013000116PBOn the market Alhydran 3ml5425013000116PBOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Feb 24, 2020	Still on market

Device identification

Trade name: Alhydran Anti Itch Care 59ml
UDI-DI code: 05425013009997
Basic UDI-DI: 5425013000116PB
Reference / catalog number: 20-31050
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: Medical hydrating cream for cooling the skin and actively reducing and relieving itching.
Additional information URL: https://www.alhydran.com/category/special-care/
Clinical sizes: 59 MU03

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05425013009997

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

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.