Organization name

MIVI Neuroscience

SRN

US-MF-000020746

Manufacturer status

Active

B293HFT110E0

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

• Do not re-use
• Do not resterilize
• Do not use if package is damaged
• Do not use past indicated date

Primary placement in Spain; available across 27 countries total.

Trade name

not provided

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

B293HFT110E0

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

B-B293HFT110E0

Reference / catalog number

HFT-110-E

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

HIBCC

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class I

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

MIVI High Flow Tubing is a sterilized and disposable medical device consisting of high-pressure PVC tubing with end fittings and an on/off switch.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• G020399EVACUATION TUBES - OTHER

• Class I medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.