Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

Back to MHRA

Manufacturer's Devices - Apple Inc

Address:

One Apple Park Way

Cupertino

CA 95014

United States

Authorised Representative/ UK Responsible Person
Name: Apple UK Ltd
Address:

100 New Bridge Street

London

London EC4V 6JA

Wales United Kingdom

Code/Term Type

Cardiac electrophysiology application software Cardiac electrophysiology application software Class IIa

Self-care monitoring/reporting software Self-care monitoring/reporting software Class IIa

Menstrual cycle self-monitoring software Menstrual cycle self-monitoring software Class I

Menstrual cycle self-monitoring software Menstrual cycle self-monitoring software Class I

Cardiac electrophysiology application software Cardiac electrophysiology application software Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Cardiac electrophysiology application software	Cardiac electrophysiology application software	Class IIa
Self-care monitoring/reporting software	Self-care monitoring/reporting software	Class IIa
Menstrual cycle self-monitoring software	Menstrual cycle self-monitoring software	Class I
Menstrual cycle self-monitoring software	Menstrual cycle self-monitoring software	Class I
Cardiac electrophysiology application software	Cardiac electrophysiology application software	Class IIa