Primary Device ID | 05060472440488 |
NIH Device Record Key | 21a98485-888c-4cfc-ac85-e1a64f3692b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tempus IC2 |
Version Model Number | 00-2001-R |
Company DUNS | 896707940 |
Company Name | REMOTE DIAGNOSTIC TECHNOLOGIES LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060472440488 [Primary] |
MWI | Monitor,Physiological,Patient(Without Arrhythmia Detection Or Alarms) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
05060472440594 | Tempus Lithium-ion Battery (Orange) |
05060472440501 | 00-2001-T |
05060472440495 | 00-2001-S |
05060472440488 | 00-2001-R |
05060472440464 | Tempus 12-Lead Electrocardiogram Harness |
05060472440457 | Glucometer Replenishment Kit |
05060472440440 | Consumables Replenishment Kit |
05060472440433 | 01-2506 |
05060472442949 | Tempus IC2 Patient Monitor |