FDA Registration Active 🇬🇧 United Kingdom

REMOTE DIAGNOSTIC TECHNOLOGIES LTD.

Reg #: 3003832357 · FEI: 3003832357 · Expires 2026
Products
19
Proprietary Names
6
Establishment Types
3
Classifications
19

Registration Details

Registration Name
REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
Registration Number
3003832357
FEI Number
3003832357
Status
Active
Expiry Year
2026
Initial Importer
No
Address
ASCENT 1, FARNBOROUGH AEROSPACE CENTRE, AEROSPACE BOULEVARD
City
FARNBOROUGH Hampshire
Country
GB

Regulatory Submissions

510(k) Number
K133988

Owner / Operator

Firm Name
REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
Operator Number
9044740
Address
ASCENT 1, FARNBOROUGH AEROSPACE CENTRE, AEROSPACE BOULEVARD
City
FARNBOROUGH
State
Hampshire
Postal Code
GU14 6XW
Country
GB
Correspondent
Rodolfo - Carollo

US Agent

Business Name
PHILIPS
Contact Name
Tami Tuttle
Address
22100 BOTHELL EVERETT HIGHWAY
City
Bothell
State
WA
ZIP
98021
Country
US
Phone
720 6821456

Products

Device Name Product Code
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) DRT
System, Measurement, Blood-Pressure, Non-Invasive DXN
Plethysmograph, Impedance DSB
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) MWI
Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase CCK
Electrocardiograph DPS
System, Imaging, Pulsed Echo, Ultrasonic IYO
Transducer, Ultrasonic, Diagnostic ITX
Oximeter DQA
Ventilatory Effort Recorder MNR
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) MHX
Dislodger, Stone, Basket, Ureteral, Metal FFL
Transmitters And Receivers, Physiological Signal, Radiofrequency DRG
Computer, Blood-Pressure DSK
Hospital Cardiac Telemetry QYW
Pacemaker, Cardiac, External Transcutaneous (Non-Invasive) DRO
Dc-Defibrillator, Low-Energy, (Including Paddles) LDD
Aid, Cardiopulmonary Resuscitation LIX
Continuous Measurement Thermometer FLL

Proprietary Names

Tempus PRO extended features Tempus PRO Accessories (Ultrasound & Video Laryngoscope probe) Tempus PRO With Enhanced Features TEMPUS LS-MANUAL Tempus Pro Patient Monitor Model numbers 00-1,00-1005,00-1006,00-1007 Tempus Pro

Establishment Types

Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility