Eckert & Ziegler

GUDID 00812444021653

Brachytherapy

RIVERPOINT MEDICAL, LLC

Brachytherapy needle
Primary Device ID00812444021653
NIH Device Record Key5b242430-9d69-4583-9156-ac48631b5042
Commercial Distribution StatusIn Commercial Distribution
Brand NameEckert & Ziegler
Version Model Number1100Y-1820X-5
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
GS100812444021653 [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 StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-02-28

On-Brand Devices [Eckert & Ziegler]

00812444027846Brachytherapy
00812444021677Brachytherapy
00812444021653Brachytherapy

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