TeleRehab Receiver Box 101127

GUDID 00856298006282

The housing used to enclose RF receiver cards for use with the TeleRehab system.

SCOTTCARE CORPORATION, THE

Electrocardiography telemetric monitoring system receiver
Primary Device ID00856298006282
NIH Device Record Key8b1a9452-7548-4eba-9e95-d27a4ae8bc19
Commercial Distribution StatusIn Commercial Distribution
Brand NameTeleRehab Receiver Box
Version Model NumberTR620
Catalog Number101127
Company DUNS808204957
Company NameSCOTTCARE CORPORATION, THE
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com
Phone216-362-0550
Emailservice@scottcare.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100856298006282 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DRGTransmitters And Receivers, Physiological Signal, Radiofrequency

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-19

Devices Manufactured by SCOTTCARE CORPORATION, THE

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