Triton Needles

GUDID 00812444027877

Brachytherapy

RIVERPOINT MEDICAL, LLC

Brachytherapy needle
Primary Device ID00812444027877
NIH Device Record Keya4ce3f42-0476-45f1-bf6c-443b89960da9
Commercial Distribution StatusIn Commercial Distribution
Brand NameTriton Needles
Version Model NumberTN 1053-1730
Company DUNS964053560
Company NameRIVERPOINT MEDICAL, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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
GS100812444027877 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, Linear, Medical

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 Date2018-02-15

On-Brand Devices [Triton Needles]

00812444027877Brachytherapy
00812444026764BRACHYTHERAPY

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