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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

ACC-INX1000A-KIT001 — Class I MDD by VIMAP TECHNOLOGIES, S.L.U

MD Atlas
VIMAP TECHNOLOGIES, S.L.U

EUDAMED last updated this device on Nov 15, 2023

ACC-INX1000A-KIT001

B-08436557390172

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: VIMAP TECHNOLOGIES, S.L.U
UDI-DI code: 08436557390172
Reference / catalog number: ACC-INX1000A-KIT001

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Manufacturer information

Organization name: VIMAP TECHNOLOGIES, S.L.U
SRN: ES-MF-000006481
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Italy		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08436557390172
Basic UDI-DI: B-08436557390172
Reference / catalog number: ACC-INX1000A-KIT001
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Accessory kit for INX-1000A. This product is an accessory of VIMAP TECHNOLOGIES devices.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039013ANGIOGRAPHIC INJECTORS

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

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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.