BRACHYTHERAPY

GUDID 00812444024968

BRACHYTHERAPY

RIVERPOINT MEDICAL, LLC

Brachytherapy needle
Primary Device ID00812444024968
NIH Device Record Keyab953b39-e746-44c0-bcaf-1c6951f50fc6
Commercial Distribution StatusIn Commercial Distribution
Brand NameBRACHYTHERAPY
Version Model Number51S-1200-1820-5
Company DUNS964053560
Company NameRIVERPOINT MEDICAL, LLC
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812444024968 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KXKSource, Brachytherapy, Radionuclide

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-02-19

On-Brand Devices [BRACHYTHERAPY]

30812444028929BRACHYTHERAPY
30812444028875Brachytherapy needle
00812444024975BRACHYTHERAPY
00812444024968BRACHYTHERAPY
00812444024951BRACHYTHERAPY
00812444024944BRACHYTHERAPY
00812444024937BRACHYTHERAPY
30812444028998Brachytherapy Needle
20812444029257Brachytherapy

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