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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

Hersubel — Class I MDR by Oxmed International BV

MD Atlas
Oxmed International BV

EUDAMED last updated this device on Mar 24, 2026

Hersubel

87207958HB-ORGNE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Oxmed International BV
UDI-DI code: 08720795808408
Reference / catalog number: F16BL

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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: Hersubel
UDI-DI code: 08720795808408
Basic UDI-DI: 87207958HB-ORGNE
Reference / catalog number: F16BL
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: HERSUBEL STEUNBANDAGE ORIGINAL 16CM BEIGE L: The Hersubel range of Support Belts are intended for use by ostomates who have a peristomal hernia, whose abdominal muscles post-surgery require extra support to prevent herniation, or who require extra support for undertaking sports activities or heavy work.
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)08720795808408

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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.

A108006ABDOMINAL OSTOMY SUPPORT BELTS

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.