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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

DOZ MED Aspirator kataru PLUS — Class IIa MDD

MD Atlas
JO-VITAL Jowita Wietecha

EUDAMED last updated this device on Jan 3, 2025

DOZ MED Aspirator kataru PLUS

B-05904988173259

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: JO-VITAL Jowita Wietecha
UDI-DI code: 05904988173259
Reference / catalog number: DOZ MED Aspirator kataru PLUS

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View device family (Basic UDI)

Manufacturer information

Organization name: JO-VITAL Jowita Wietecha
SRN: PL-MF-000035181
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Jan 17, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05904988173259
Basic UDI-DI: B-05904988173259
Reference / catalog number: DOZ MED Aspirator kataru PLUS
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
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)05904988173259

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

R05010302DOUBLE-CHAMBER MUCOUS MEMBRANE ASPIRATORS

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.

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