Type-S™ Lok-Bar™ MTWBL001

GUDID 00841439113882

For use with TotalRT All In One Solution and Type-S™ Overlays and Extensions

MEDTEC, INC.

Radiological breast positioner, non-wearable
Primary Device ID00841439113882
NIH Device Record Key174e9738-796d-42be-bc66-0e1842fd2c59
Commercial Distribution StatusIn Commercial Distribution
Brand NameType-S™ Lok-Bar™
Version Model NumberMTWBL001
Catalog NumberMTWBL001
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100841439113882 [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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-23
Device Publish Date2022-05-13

Devices Manufactured by MEDTEC, INC.

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00841439114681 - Pronumbra2025-09-22 Pronumbra 130cm kVue
00841439114698 - Pronumbra2025-09-22 Pronumbra Neck Support, 40mm
00841439114704 - Pronumbra2025-09-22 Pronumbra Neck Support, 50mm
00841439114711 - Pronumbra2025-09-22 Pronumbra Neck Support, 65mm
00841439114728 - Pronumbra2025-09-22 Pronumbra Shoulder Adapter
00841439114841 - ZiFix Traverse2025-09-22 ZiFix Traverse with ONEClamp

Trademark Results [Type-S]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TYPE-S
TYPE-S
76669344 3531430 Dead/Cancelled
NEC CASIO MOBILE COMMUNICATIONS, LTD.
2006-11-21

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