EU to reportedly start China probe over medical device procurement
The inquiry arrives against a backdrop of increasingly tenuous EU-China relations.
16 April 2024
16 April 2024
The inquiry arrives against a backdrop of increasingly tenuous EU-China relations.
The GUARDIAN-Heart trial consisted of 1,261 US adult patients and saw 32% drop in the use of post-transplant mechanical circulatory support.
The US Food and Drug Administration (FDA) has cleared Sight Sciences’ OMNI surgical system to reduce intraocular pressure in patients with primary open-angle glaucoma.
Mice treated with the device exhibited significantly reduced tumour sizes when compared to the untreated cohort.
The VSP PEEK Cranial Implant includes segmentation and 3D modeling software, Evonik VESTAKEEP i4 3DF PEEK.
The OviTex IHR is intended to address the need for a more natural repair in inguinal hernia procedures.
The submission follows the ICE3 clinical trial results that showed a 96.3% recurrence-free rate at five years.
The test, which can measure GFAP from a simple blood draw, is now made available nationwide.
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