Home » MHRA Releases Guidance on Remanufacturing Single-Use Devices
MHRA Releases Guidance on Remanufacturing Single-Use Devices
Devicemakers in the UK that remanufacture single-use devices must accept all the obligations and liabilities that an original manufacturer would face, the regulator said.
The UK’s Medicines & Healthcare products Regulatory Agency issued its first formal guidance on remanufacturing single-use devices; however, it notes that the medical device directives “do not explicitly permit remanufacturing or reprocessing.”
Although single-use devices may be manufactured in the UK, the remanufacturer must ensure that the intended use of the device is the same as the original product.
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