Patient Hand Grip MTIL662502

GUDID 00841439106389

For use with Universal Couchtop™

MEDTEC, INC.

Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system
Primary Device ID00841439106389
NIH Device Record Key178ae4c3-6b11-4ab6-a4b4-c17a61e9a960
Commercial Distribution StatusIn Commercial Distribution
Brand NamePatient Hand Grip
Version Model NumberMTIL662502
Catalog NumberMTIL662502
Company DUNS103977526
Company NameMEDTEC, INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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

Device Dimensions

Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch
Length7.91 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100841439106389 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IXQTable, radiographic, stationary top

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2020-03-31
Device Publish Date2017-08-02

On-Brand Devices [Patient Hand Grip]

00841439107287Patient Hand Grip - Left
00841439106389For use with Universal Couchtop™
00841439106372For use with Universal Couchtop™

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.