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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

oxiSperm II — IVDD — General IVDD by Halotech DNA

MD Atlas
Halotech DNA

EUDAMED last updated this device on May 25, 2022

oxiSperm II

B-08437024427032

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Halotech DNA
UDI-DI code: 08437024427032
Reference / catalog number: HT-OS20II

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Manufacturer information

Organization name: Halotech DNA
SRN: ES-MF-000001921
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW011
Do not touch the membrane directly with the hands or skin. This can modify the expected reaction. Avoid direct exposure of the reactive membrane to sunlight. Keep the unused reactive membranes in the wrapper protected from light.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: oxiSperm II
UDI-DI code: 08437024427032
Basic UDI-DI: B-08437024427032
Reference / catalog number: HT-OS20II
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Kit for measurement of prooxidant activity in sperm samples
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W01019099CLINICAL CHEMISTRY REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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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.