15 Dicembre 2018
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Selected participants will work directly with the FDA to accelerate the development of and eventual review of marketing applications for these innovative products. Read more: https://go.usa.gov/xPMPk pic.twitter.com/6rRnfSyLy4

Redazione Redazione
(AGENPARL) – Silver Spring ven 30 novembre 2018 [unable to retrieve full-text content]. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical
Agenparl English Salute Sociale

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.usa.gov/xPMEK  #MedicalDevicepic.twitter.com/M55ddC98wW

Redazione Redazione
(AGENPARL) – Silver Spring ven 30 novembre 2018 [unable to retrieve full-text content]. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical
Agenparl English Salute Sociale

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq3Yw0b

Redazione Redazione
(AGENPARL) – Silver Spring ven 30 novembre 2018 [unable to retrieve full-text content]. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical

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