Bath Liner MTCBPLLG

GUDID 00841439104101

48 x 76cm

MEDTEC, INC.

Thermoplastic-moulding water bath
Primary Device ID00841439104101
NIH Device Record Key49dcaa69-20cb-4414-a757-35749eaffc59
Commercial Distribution StatusIn Commercial Distribution
Brand NameBath Liner
Version Model NumberMTCBPLLG
Catalog NumberMTCBPLLG
Company DUNS103977526
Company NameMEDTEC, INC.
Device Count2
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

Device Dimensions

Length30 Inch
Length30 Inch
Length30 Inch
Length30 Inch
Length30 Inch
Length30 Inch
Length30 Inch
Length30 Inch
Length30 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100841439104101 [Primary]
GS110841439104108 [Unit of Use]

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 Date2020-03-27
Device Publish Date2017-08-02

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