Triton Needles

GUDID 00812444026764

BRACHYTHERAPY

RIVERPOINT MEDICAL, LLC

Brachytherapy needle
Primary Device ID00812444026764
NIH Device Record Keydef99cbe-edd8-4d71-8a76-822abf4b0dc0
Commercial Distribution StatusIn Commercial Distribution
Brand NameTriton Needles
Version Model NumberTN 1031-1820
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812444026764 [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 Date2017-07-27

On-Brand Devices [Triton Needles]

00812444027877Brachytherapy
00812444026764BRACHYTHERAPY

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