Transflux MRI 150

Organization name

BHL-Medical, Indústria de Produtos Hospitalares, lda

SRN

PT-MF-000002811

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  Do not exceed the pressure of 300 Psi. The use of higher pressure or occlusions in the fluid path might result into leaks or ruptures.

Primary placement in Portugal; available across 10 countries total.

Trade name

Transflux MRI 150

UDI-DI code

05600988820505

Basic UDI-DI

56009888TD001TFMRIHT

Reference / catalog number

PR-20206

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Intended for administration of contrast media into the human body in MRI imaging procedures, for the purpose of diagnosis in combination with an automatic injector.

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.

• A03020101LOW PRESSURE EXTENSION LINES