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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

700125 — Class I MDR by Vital Pro Kft.

MD Atlas
Vital Pro Kft.

EUDAMED last updated this device on Nov 14, 2024

700125

59991300REF700120VN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vital Pro Kft.
UDI-DI code: 05999130000019
Reference / catalog number: 700125

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Manufacturer information

Organization name: Vital Pro Kft.
SRN: HU-MF-000028773
Manufacturer status: Active

Related devices

70012859991300REF700120VNOn the market 70012659991300REF700120VNOn the market 70012759991300REF700120VNOn the market 70012459991300REF700120VNOn the market

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.

Market distribution

Primary placement in Hungary; available across 2 countries total.

Country	On market since	Until
HungaryPrimary placement	Nov 14, 2024	Still on market
Romania	Nov 14, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999130000019
Basic UDI-DI: 59991300REF700120VN
Reference / catalog number: 700125
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 42 MU10

EMDN nomenclature code(s)

Y122106REAR SELF-PROPELLED WHEELCHAIRS

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