BHL-Hiflow

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 1200 Psi. The use of higher pressure or occlusions in the fluid path might result into leaks or ruptures.

Primary placement in Portugal; available across 2 countries total.

Trade name

BHL-Hiflow

UDI-DI code

05600988830023

Basic UDI-DI

56009888TF002KW

Reference / catalog number

BHL-HFMF-120

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 by High pressure, into the human body, in 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.

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

• A03020102HIGH PRESSURE EXTENSION LINES