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

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Manufacturer's Devices - Etymotic Research Inc.

Address:

61 Martin Lane

Elk Grove Village IL

60007

United States

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Class I

Analytical non-scalp cutaneous electrode Analytical non-scalp cutaneous electrode Class I

Audiometric ear tip Audiometric ear tip Class I

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
Analytical non-scalp cutaneous lead	Analytical non-scalp cutaneous lead	Class I
Analytical non-scalp cutaneous electrode	Analytical non-scalp cutaneous electrode	Class I
Audiometric ear tip	Audiometric ear tip	Class I