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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

700128 — Class I MDR by Vital Pro Kft.

MD Atlas
Vital Pro Kft.

EUDAMED last updated this device on Nov 14, 2024

700128

59991300REF700120VN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vital Pro Kft.
UDI-DI code: 05999130000040
Reference / catalog number: 700128

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Manufacturer information

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

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: 05999130000040
Basic UDI-DI: 59991300REF700120VN
Reference / catalog number: 700128
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: 52 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

Related devices

70012659991300REF700120VNOn the market 70012559991300REF700120VNOn 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.