BRACHYTHERAPY NEEDLE

GUDID 00812444026399

BRACHYTHERAPY

RIVERPOINT MEDICAL, LLC

Brachytherapy needle Brachytherapy needle
Primary Device ID00812444026399
NIH Device Record Key76c70638-e7d6-4622-a319-913926400e7c
Commercial Distribution StatusIn Commercial Distribution
Brand NameBRACHYTHERAPY NEEDLE
Version Model Number1150-1730-1
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812444026399 [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 Date2017-08-22

On-Brand Devices [BRACHYTHERAPY NEEDLE]

00812444027006BRACHYTHERAPY
00812444026993BRACHYTHERAPY
00812444026399BRACHYTHERAPY
00812444026382BRACHYTHERAPY
30812444029285Brachytherapy Needle
10810020082194Brachytherapy
10810020082187Brachytherapy

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