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 - IRADIMED CORPORATION

Address:

1025 WILLA SPRINGS DRIVE

WINTER SPRNGS

FLORIDA 32708

United States

Authorised Representative/ UK Responsible Person
Name: Medical Device Consultancy Ltd
Address:

7 Pinewood Drive Ashley Heath

Market Drayton

Market Drayton

TF9 4PA

England United Kingdom

Code/Term Type

Bedside infusion pump single-channel Bedside infusion pump single-channel Class IIb

Electric infusion pump administration set single-use Electric infusion pump administration set single-use Class IIa

Electrocardiographic electrode single-use Electrocardiographic electrode single-use Class I

MRI-patient physiologic monitoring system MRI-patient physiologic monitoring system Class IIb

Intravenous pole Intravenous pole 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
Bedside infusion pump single-channel	Bedside infusion pump single-channel	Class IIb
Electric infusion pump administration set single-use	Electric infusion pump administration set single-use	Class IIa
Electrocardiographic electrode single-use	Electrocardiographic electrode single-use	Class I
MRI-patient physiologic monitoring system	MRI-patient physiologic monitoring system	Class IIb
Intravenous pole	Intravenous pole	Class I