Guider Softip™ XF

GUDID 08714729244295

Guide Catheter

BOSTON SCIENTIFIC CORPORATION

Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use
Primary Device ID08714729244295
NIH Device Record Key39f77d1f-6e8d-4d80-886a-9f3be68b88f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameGuider Softip™ XF
Version Model NumberM003101420
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 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
GS108714729244295 [Primary]

FDA Product Code

DQYCATHETER, PERCUTANEOUS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-07-23
Device Publish Date2016-09-24

On-Brand Devices [Guider Softip™ XF]

08714729283553Guide Catheter
08714729283546Guide Catheter
08714729283539Guide Catheter
08714729283522Guide Catheter
08714729283515Guide Catheter
08714729283508Guide Catheter
08714729244394Guide Catheter
08714729244387Guide Catheter
08714729244370Guide Catheter
08714729244356Guide Catheter
08714729244349Guide Catheter
08714729244332Guide Catheter
08714729244318Guide Catheter
08714729244301Guide Catheter
08714729244295Guide Catheter
08714729202561Guide Catheter
08714729202554Guide Catheter
08714729202547Guide Catheter
08714729202523Guide Catheter
08714729202516Guide Catheter
08714729202509Guide Catheter
08714729202486Guide Catheter
08714729202479Guide Catheter
08714729202462Guide Catheter

Trademark Results [Guider Softip]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GUIDER SOFTIP
GUIDER SOFTIP
76330341 2800935 Live/Registered
STRYKER CORPORATION
2001-10-25
GUIDER SOFTIP
GUIDER SOFTIP
76330341 2800935 Live/Registered
STRYKER NV OPERATIONS LIMITED
2001-10-25

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