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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

20F100061 — Class I MDR by Medinovitas Kft

MD Atlas
Medinovitas Kft

EUDAMED last updated this device on Jul 1, 2024

20F100061

599957142M030101C9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medinovitas Kft
UDI-DI code: 05999571421220
Reference / catalog number: 20F100061

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Manufacturer information

Organization name: Medinovitas Kft
SRN: HU-MF-000007416
Manufacturer status: Active

Related devices

20F100041599957142M030101C9On the market 23F100101599957142M030101C9On the market 23F100101L599957142M030101C9On the market 23F100151L599957142M030101C9On the market 23F100041L599957142M030101C9On the market

Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05999571421220
Basic UDI-DI: 599957142M030101C9
Reference / catalog number: 20F100061
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: Benda di garza 10mx6cm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030101HYDROPHILIC GAUZE BANDAGES

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.