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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

DECCS 23 AAV-VE — Class I MDR by MEDIVAC S.R.L. SOCIETA'…

MD Atlas
MEDIVAC S.R.L. SOCIETA' BENEFIT

EUDAMED last updated this device on May 24, 2024

DECCS 23 AAV-VE

805368965DECCSFD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIVAC S.R.L. SOCIETA' BENEFIT
UDI-DI code: 18053689650126
Reference / catalog number: DECCS 23 AAV-VE

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Manufacturer information

Organization name: MEDIVAC S.R.L. SOCIETA' BENEFIT
SRN: IT-MF-000030012
Manufacturer status: Active

Related devices

AAV14805368965AAV23CZOn the market MV23A805368965AAV23CZOn the market DECCS 14 ST805368965DECCSFDOn the market DECCS 14 AAV-CO805368965DECCSFDOn the market DECCS 14 AAV-VE805368965DECCSFDOn the market

Critical warnings

No critical warnings reported for this device.

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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: 18053689650126
Basic UDI-DI: 805368965DECCSFD
Reference / catalog number: DECCS 23 AAV-VE
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: 25
Additional product description: Kit per la raccolta di esalato condensato da utilizzare con gli strumenti Turbo 23 e AAV 23 e con pazienti non collaborativi e ventilati
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

EMDN nomenclature code(s)

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

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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.