GUDID 08714729035404

Arterial Entry Needle

BOSTON SCIENTIFIC CORPORATION

Vascular catheter introduction needle
Primary Device ID08714729035404
NIH Device Record Key1ce25d86-40cb-46bd-972b-e1d733b70352
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberM001441660
Company DUNS021717889
Company NameBOSTON SCIENTIFIC CORPORATION
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS108714729035404 [Package]
Contains: 08714729739258
Package: [10 Units]
In Commercial Distribution
GS108714729739258 [Primary]

FDA Product Code

FMINeedle, hypodermic, single lumen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2024-06-06
Device Publish Date2016-09-24

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

08714729424260 - Contour™2024-09-11 Ureteral Stent Set
08714729462583 - Contour™2024-09-11 Ureteral Stent Set
08714729462651 - Contour™2024-09-11 Ureteral Stent Set
08714729462798 - Contour™2024-09-11 Ureteral Stent Set
00191506020798 - RHYTHMIA HDx™2024-09-11 Ablation Connection Box - IntellaNav StablePoint™ (for INTELLAGEN™)
00191506020804 - RHYTHMIA HDx™2024-09-11 Ablation Connection Box (for INTELLAGEN™)
08714729010975 - Connector2024-09-09 FOR 7F THROUGH 10F CATHETERS WITH LUER LOCK FITTING Ureteral Catheter Connector
08714729010982 - Connector2024-09-09 FOR 3F THROUGH 6F CATHETERS WITH LUER LOCK FITTING Ureteral Catheter Connector

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.