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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

ANA Advanced Neurovascular Access™ — Class III MDD

MD Atlas
ANACONDA BIOMED, S.L.

EUDAMED last updated this device on Sep 27, 2022

ANA Advanced Neurovascular Access™

B-ANA-1-00001N7

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ANACONDA BIOMED, S.L.
UDI-DI code: D-ANA-1-00001N7
Reference / catalog number: 1-00001

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Manufacturer information

Organization name: ANACONDA BIOMED, S.L.
SRN: ES-MF-000009187
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 1, 2020	Still on market

Device identification

Trade name: ANA Advanced Neurovascular Access™
UDI-DI code: D-ANA-1-00001N7
Basic UDI-DI: B-ANA-1-00001N7
Reference / catalog number: 1-00001
Issuing entity: EUDAMED

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The ANA Advanced Neurovascular Access™ Device (ANA device or ANA system) is a distal access catheter system designed to assist in neurovascular procedures by facilitating the insertion and guiding of other devices (i.e. retrieval devices and intravascular catheters) and restricting blood flow at the target position. It is a sterile, single use, disposable intravascular device comprised of two coaxial catheters (a delivery catheter and a funnel catheter) consisting of sections with variable stiffness. The funnel catheter is comprised of a radiopaque nitinol braid (a self-expanding funnel) covered by a continuous silicone coating that provides temporary local flow restriction when deployed. The delivery catheter has a hydrophilic coating to reduce friction during use and a radiopaque marker at the distal end. Both catheters have Luer lock hubs on their proximal ends.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C01020101CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS

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

1-000038437019519ANAB6On 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.