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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

Secuthin — Class I MDR by Oxmed International BV

MD Atlas
Oxmed International BV

EUDAMED last updated this device on Mar 17, 2026

Secuthin

87207958WSC7X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Oxmed International BV
UDI-DI code: 08720795809337
Reference / catalog number: WSC50

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View device family (Basic UDI)

Manufacturer information

Organization name: Oxmed International BV
SRN: NL-MF-000025538
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.

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

Device identification

Trade name: Secuthin
UDI-DI code: 08720795809337
Basic UDI-DI: 87207958WSC7X
Reference / catalog number: WSC50
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: Secuthin Skin Barrier Cream: The Secuthin Skin Barrier Cream is an aqueous based, white, easy flowing cream without perfume. The Secuthin Skin Barrier Cream is designed for use by ostomy device users to provide a protective layer between the stoma adhesive and the skin. Applied prior to adhesion of the stoma collection device it will not affect the integrity of the hydrocolloid adhesion properties. It is intended to be massaged well into the skin before adhesion of the hydrocolloid baseplate of the stoma appliance. The Secuthin Skin Barrier Cream has been used in conjunction with different types of hydrocolloid and found to be compatible. The Secuthin Skin Barrier Cream contains two common preservatives – Paraben and Phenoxyethanol.
Additional information URL: https://oxmed.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720795809337

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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.

A108002PROTECTIVE CREAMS / GELS FOR PERISTOMAL SKIN

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.