Legacy device under Class A sterile devices

#1
Dear Team,

I am India based manufacturer of lab devices. To capture EU market, I have appointed EU authorized representative from Europe for IVD products to sell over there.
I have a couple of Class A sterile consumables, which were already approved and registered as per 98/79/ EC before 24th May 2022 by our EU rep.
On that ground, could I sell the devices under legacy devices without notification body involvement until 26th May 2027?
I agree that after May 2027, I have to appoint the notification body for compliance as per 2017/746.
I have also referred the MDCG-8 May 2022 but still, I am not able to conclude the same.

Looking forward to your reply.

Thanks,
Compliance
 
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