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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

AIVIA — Class I MDR by PYRESCOM

MD Atlas
PYRESCOM

EUDAMED last updated this device on Jul 21, 2025

AIVIA

37700AIVIA-V3-2005A

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PYRESCOM
UDI-DI code: 03770023276023
Reference / catalog number: X3A200-XX101

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Manufacturer information

Organization name: PYRESCOM
SRN: FR-MF-000007671
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: AIVIA
UDI-DI code: 03770023276023
Basic UDI-DI: 37700AIVIA-V3-2005A
Reference / catalog number: X3A200-XX101
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: Public access defibrillator cabinet, designed to house and secure an Automated External Defibrillator (AED) in public spaces, establishments open to the public, as well as in residential or commercial premises, in order to allow rapid access to the device in the event of a cardiac emergency.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C020480CARDIOVERSION AND EXTERNAL DEFIBRILLATION DEVICES - ACCESSORIES

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

AIVIA37700AIVIA-V3-2105DOn 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.