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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

Vereya — Class I MDR by NIPI-M AD

MD Atlas
NIPI-M AD

EUDAMED last updated this device on Mar 2, 2023

Vereya

3800600VG1-000BGWY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NIPI-M AD
UDI-DI code: 03800600004784
Reference / catalog number: 300002/IZ

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Manufacturer information

Organization name: NIPI-M AD
SRN: BG-MF-000033684
Manufacturer status: Active

Market distribution

Primary placement in Bulgaria; available across 1 country total.

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

Device identification

Trade name: Vereya
UDI-DI code: 03800600004784
Basic UDI-DI: 3800600VG1-000BGWY
Reference / catalog number: 300002/IZ
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: Легло за използване в домашни условия , болница или друго медицинско заведение.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080699MEDICAL BEDS - OTHER

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

Vereya ECO3800600VEG1-000BGF9On the market Vereya ECO 803800600VEG180-000BGZDOn the market Vereya Plus3800600VG1-000BGWYOn the market Vereya Plus 803800600VG180-000BG9XOn 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.