Pinpoint GT 9770642

GUDID 30801741128876

Pinpoint GT Needle

Bard Access Systems, Inc.

Peripheral nerve-block sharp needle
Primary Device ID30801741128876
NIH Device Record Keyaed3800b-7318-43a0-981b-2d7907ddc6b8
Commercial Distribution StatusIn Commercial Distribution
Brand NamePinpoint GT
Version Model Number9770642
Catalog Number9770642
Company DUNS044611812
Company NameBard Access Systems, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com

Device Dimensions

Length2.75 Inch
Length2.75 Inch
Length2.75 Inch
Length2.75 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741128875 [Primary]
GS110801741128872 [Package]
Contains: 00801741128875
Package: CA [20 Units]
In Commercial Distribution
GS130801741128876 [Package]
Contains: 10801741128872
Package: BX [4 Units]
In Commercial Distribution

FDA Product Code

BSPNEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-10-04

On-Brand Devices [Pinpoint GT]

30801741128937Hypodermic Pinpoint GT Needle
30801741128920Hypodermic Pinpoint GT Needle
10801741128919Pinpoint GT Needle
10801741128902Hypodermic Pinpoint GT Needle
30801741128890Pinpoint GT Needle
30801741128883Hypodermic Pinpoint GT Needle
30801741128876Pinpoint GT Needle
30801741128869Pinpoint GT Needle
30801741128852Pinpoint GT Needle

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.