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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 15ml — Class I MDR by BAP Medical B.V.

MD Atlas
BAP Medical B.V.

EUDAMED last updated this device on Apr 7, 2026

Alhydran 15ml

5425013000116PB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BAP Medical B.V.
UDI-DI code: 05425013000130
Reference / catalog number: 20-10015

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View device family (Basic UDI)

Manufacturer information

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

Critical warnings

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

CW010
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	Aug 11, 2011	Still on market

Device identification

Trade name: Alhydran 15ml
UDI-DI code: 05425013000130
Basic UDI-DI: 5425013000116PB
Reference / catalog number: 20-10015
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. Ensures optimal, long-lasting hydration and prevents moisture loss. Ideal for treatment of disrupted skin barrier. Suitable for (after)care of burn wounds, treatment and prevention of scars, treatment of (extremely) dry skin and reduction of redness and itching.
Additional information URL: https://www.alhydran.com/products/alhydran/
Clinical sizes: 15 MU03

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05425013000130

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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.