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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

Weldra — Class I MDR by Oxmed International BV

MD Atlas
Oxmed International BV

EUDAMED last updated this device on Mar 17, 2026

Weldra

87207958WMNZ-NSDT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Oxmed International BV
UDI-DI code: 08720795800419
Reference / catalog number: WMNZ2000

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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: Weldra
UDI-DI code: 08720795800419
Basic UDI-DI: 87207958WMNZ-NSDT
Reference / catalog number: WMNZ2000
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: 10
Additional product description: Weldra Urine (Night Drainage) Bag Non-Sterile 2000ml: The 2000ml capacity Weldra Urine Bag is for use as a urine collection bag and can be connected to most urostomy pouches and urine leg bag systems via the attached universal connector. The Weldra Urine Bag is supplied non-sterile for use by individuals who require extra capacity for night time bladder drainage. Included with each Weldra Urine Bag is a hanging frame with fastening cord, bed sheet clamp, and tube clamp. The Weldra Urine Bag shows measurement graduations on one side of the bag, but these are for guidance only and are not precise measurements. Emptying of the Weldra Urine Bag can be done using one hand via the emptying valve at the base of the bag.
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)08720795800419

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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.

A06030301URINE COLLECTION BAGS

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.