Echo ECHO100100-01

GUDID 07613327624069

Intracranial Base Catheter

Stryker Corporation

Vascular guide-catheter, single-use
Primary Device ID07613327624069
NIH Device Record Key3852b18e-bf87-46a8-9721-5bebd4f4b173
Commercial Distribution StatusIn Commercial Distribution
Brand NameEcho
Version Model NumberECHO100100-01
Catalog NumberECHO100100-01
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

Device Dimensions

Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch
Length100 Centimeter
Lumen/Inner Diameter0.1 Inch

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.

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327624069 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QJPCatheter, Percutaneous, Neurovasculature

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-03
Device Publish Date2025-01-24

On-Brand Devices [Echo]

07613327624083Intracranial Base Catheter
07613327624069Intracranial Base Catheter

Trademark Results [Echo]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ECHO
ECHO
98828502 not registered Live/Pending
Valor Offroad, LLC
2024-10-30
ECHO
ECHO
98797427 not registered Live/Pending
Innova Electronics Corporation
2024-10-11
ECHO
ECHO
98738129 not registered Live/Pending
MlilyUSA, Inc.
2024-09-06
ECHO
ECHO
98714109 not registered Live/Pending
Coulter Ventures, LLC
2024-08-23
ECHO
ECHO
98589066 not registered Live/Pending
Echo Technologies LLC
2024-06-06
ECHO
ECHO
98403638 not registered Live/Pending
Stylecraft, LLC
2024-02-13
ECHO
ECHO
98298155 not registered Live/Pending
Ncardia B.V.
2023-12-04
ECHO
ECHO
98242300 not registered Live/Pending
Foamtec International Co., Ltd.
2023-10-26
ECHO
ECHO
98133210 not registered Live/Pending
Autism Solutions, Inc.
2023-08-15
ECHO
ECHO
98092120 not registered Live/Pending
Tulster, LLC
2023-07-19
ECHO
ECHO
98020509 not registered Live/Pending
Eastward Partners
2023-05-31
ECHO
ECHO
97868610 not registered Live/Pending
Yen, Weixi
2023-04-01

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