BIOPSY NEEDLE

GUDID 10812444022954

BIOPSY NEEDLE

RIVERPOINT MEDICAL, LLC

Prostate biopsy needle Prostate biopsy needle
Primary Device ID10812444022954
NIH Device Record Keyffd401fd-975d-4702-bf39-90c9fe442496
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIOPSY NEEDLE
Version Model NumberRPM1000-1820
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812444022957 [Primary]
GS110812444022954 [Package]
Contains: 00812444022957
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KNWInstrument, Biopsy

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 Date2015-10-22

On-Brand Devices [BIOPSY NEEDLE]

00812444024920BRACHYTHERAPY
00812444024913BRACHYTHERAPY
10812444022954BIOPSY NEEDLE
00812444022926BIOPSY NEEDLE
00812444022308BIOPSY NEEDLE
30812444029148Biopsy Needle
30812444029131Biopsy Needle

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