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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

VST DG 01 — Class I MDR by SC VESTA INVESTMENT SRL

MD Atlas
SC VESTA INVESTMENT SRL

EUDAMED last updated this device on Oct 25, 2022

VST DG 01

5944759081DESCHIZATORTF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SC VESTA INVESTMENT SRL
UDI-DI code: 05944759081116
Reference / catalog number: VST DG 01

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View device family (Basic UDI)

Manufacturer information

Organization name: SC VESTA INVESTMENT SRL
SRN: RO-MF-000028779
Manufacturer status: Active

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VST AT 025944759081ATELAFAOn the market VST BS 015944759081BATISTAZ5On the market DISPOZITIV INTERMEDIAR5944759081DISPOZITIVDTOn the market VSTG5944759081GAROUGROn the market VST PG 105944759081CANULAADULTIPHOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05944759081116
Basic UDI-DI: 5944759081DESCHIZATORTF
Reference / catalog number: VST DG 01
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: Dispozitiv medical destinat deschiderii gurii inclestate a accidentatilor pentru a crea conditiile acordarii primului ajutor.
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)05944759081116

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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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.