MedWatch

FDA clears Ambu's new bronchoscope generation

The Danish medtech firm is now authorized to sell its newest generation of single-use bronchoscopes both in the EU and the US.

Photo: PR / Ambu

After obtaining the EU’s CE mark for the Ascope 5 Broncho device in May, medtech firm Ambu can now also launch in the US, according to a Tuesday press release.

The US Food and Drug Administration (FDA) has approved the single-use bronchoscope portfolio, which the firm says has more advanced imaging features due to a new high-resolution camera chip.

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