CoAccess™

GUDID 08714729349570

Introducer Set

BOSTON SCIENTIFIC CORPORATION

Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use
Primary Device ID08714729349570
NIH Device Record Key9ac2558a-cfb9-4547-9b01-bd179b915697
Commercial Distribution StatusIn Commercial Distribution
Brand NameCoAccess™
Version Model NumberM001262250
Company DUNS021717889
Company NameBOSTON SCIENTIFIC CORPORATION
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS108714729349570 [Primary]

FDA Product Code

GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-06-10
Device Publish Date2016-09-24

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

00191506034429 - RHYTHMIA HDx™2024-03-11 Ablation Connection Box
00191506020408 - IntellaNav StablePoint™ Cable2024-03-08 Catheter Cable
08714729419396 - Percuflex™2024-03-08 Ureteral Stent
08714729992233 - INTELLANAV STABLEPOINT™2024-03-08 Ablation Catheter
08714729992240 - INTELLANAV STABLEPOINT™2024-03-08 Ablation Catheter
00191506019570 - Rubicon™ Control2024-02-26 Support Catheter
00191506019594 - Rubicon™ Control2024-02-26 Support Catheter
00191506019617 - Rubicon™ Control2024-02-26 Support Catheter

Trademark Results [CoAccess]

Mark Image

Registration | Serial
Company
Trademark
Application Date
COACCESS
COACCESS
77607168 3717640 Live/Registered
Council on Accreditation of Nurse Anesthesia Educational Programs
2008-11-04
COACCESS
COACCESS
76388232 not registered Dead/Abandoned
OPTICAL ACCESS OAL LTD.
2002-03-26
COACCESS
COACCESS
76048328 3261363 Live/Registered
BOSTON SCIENTIFIC SCIMED, INC.
2000-05-15

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