TRANSFORM SRC0420

GUDID 07613327004458

C Compliant Occlusion Balloon Catheter

Stryker Corporation

Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided
Primary Device ID07613327004458
NIH Device Record Key9ed92f17-1e27-4f32-a6ca-5f018c37fd75
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRANSFORM
Version Model NumberM003SRC04200
Catalog NumberSRC0420
Company DUNS042405446
Company NameStryker 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

Customer Support Contacts

Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com
Phone+1(855)916-3876
EmailNVCustomerService@stryker.com

Device Dimensions

Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
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Length20 Millimeter
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Length20 Millimeter
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Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry, dark place.

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327004458 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MJNCatheter, intravascular occluding, temporary

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-03-21
Device Publish Date2016-09-21

On-Brand Devices [TRANSFORM]

07613327004717SC Super Compliant Occlusion Balloon Catheter
07613327004700SC Super Compliant Occlusion Balloon Catheter
07613327004694SC Super Compliant Occlusion Balloon Catheter
07613327004687C Compliant Occlusion Balloon Catheter
07613327004526SC Super Compliant Occlusion Balloon Catheter
07613327004519SC Super Compliant Occlusion Balloon Catheter
07613327004502SC Super Compliant Occlusion Balloon Catheter
07613327004496C Compliant Occlusion Balloon Catheter
07613327004489C Compliant Occlusion Balloon Catheter
07613327004472C Compliant Occlusion Balloon Catheter
07613327004465C Compliant Occlusion Balloon Catheter
07613327004458C Compliant Occlusion Balloon Catheter
07613327004441C Compliant Occlusion Balloon Catheter
07613327004434C Compliant Occlusion Balloon Catheter
07613327004427C Compliant Occlusion Balloon Catheter
07613327004410C Compliant Occlusion Balloon Catheter

Trademark Results [TRANSFORM]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRANSFORM
TRANSFORM
98316227 not registered Live/Pending
Water Pik, Inc.
2023-12-15
TRANSFORM
TRANSFORM
98045041 not registered Live/Pending
AS America, Inc.
2023-06-15
TRANSFORM
TRANSFORM
90597436 not registered Live/Pending
American Sports Licensing, LLC
2021-03-23
TRANSFORM
TRANSFORM
90461135 not registered Live/Pending
Ramsden, Jean A
2021-01-12
TRANSFORM
TRANSFORM
90461135 not registered Live/Pending
Matthew Ramsden
2021-01-12
TRANSFORM
TRANSFORM
88900244 not registered Live/Pending
TransFORM
2020-05-04
TRANSFORM
TRANSFORM
88863992 not registered Live/Pending
Cudanin, Vicki L.
2020-04-08
TRANSFORM
TRANSFORM
88490571 not registered Live/Pending
MEET HEAD BRANDS, LLC
2019-06-26
TRANSFORM
TRANSFORM
88487923 not registered Live/Pending
Gatherlab
2019-06-25
TRANSFORM
TRANSFORM
88469702 not registered Live/Pending
Gambro Lundia AB
2019-06-12
TRANSFORM
TRANSFORM
88306740 not registered Dead/Abandoned
Statflo Inc.
2019-02-19
TRANSFORM
TRANSFORM
87705891 not registered Live/Pending
GRAHAM & BROWN LIMITED
2017-12-02

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