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mahamad shafi S S
RA
August 2019
Is there any specific time line to update the labels for the *Class* *I* and *Ir* devices.
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Is there any specific time line to update the labels including the UDI/human readable requirements for the *Class* *I* and *Ir* devices.

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Asked on August 8, 2019 10:21 pm
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mahamad shafi S S

Hi, anybody could answer me please

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Michelle Lott, RAC

Hi Mahamad
Unfortunately Class I and Ir both have to be fully compliant to the MDR by May 26, 2020. There are to "rubs" here:
1) you can comply with UDI if the EU commission doesn't have their ducks in a row with the database.
2) 1r involves a notified body involvement. As you know they're are only two designated at the moment and a hard brexit could leave us with just one. Supposedly the EU will designated 20 more by the end of 2019 but who knows?! It took them 24 months to designated the two they have. There may not be enough that can do the work by May!

Raimund Laqua at www.eudamed.eu will be able to look in the crystal ball and answer your UDI questions a bit better. (That website is his own business because the EU did so little planning for Eudamed they did not even buy the domain. Tell him Michelle sent you.)

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mahamad shafi S S

Thanks Michelle

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