Respiratory Plate MTSBRT003

GUDID 00841439107256

Respiratory Plate

MEDTEC, INC.

Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner Radiological whole-body positioner
Primary Device ID00841439107256
NIH Device Record Key6682040e-b830-4d23-84df-1d40364be9ba
Commercial Distribution StatusIn Commercial Distribution
Brand NameRespiratory Plate
Version Model NumberMTSBRT003
Catalog NumberMTSBRT003
Company DUNS103977526
Company NameMEDTEC, INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com

Device Dimensions

Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch
Width6.5 Inch
Length5.1 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100841439107256 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, linear, medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-05-30
Device Publish Date2017-08-02

On-Brand Devices [Respiratory Plate]

00841439110447Respiratory Plate
00841439107256Respiratory Plate

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