AquaPulse® Auxiliary Water Connector

GUDID 14897106950529

GA Health Company Limited

Surgical irrigation tubing set, single-use Surgical irrigation tubing set, single-use Surgical irrigation tubing set, single-use Surgical irrigation tubing set, single-use Surgical irrigation tubing set, single-use Surgical irrigation tubing set, single-use Surgical irrigation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use
Primary Device ID14897106950529
NIH Device Record Key7c1592f0-916e-4e52-b10c-d7ade8149812
Commercial Distribution StatusIn Commercial Distribution
Brand NameAquaPulse® Auxiliary Water Connector
Version Model NumberGAR064
Company DUNS686908512
Company NameGA Health Company Limited
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104897106950522 [Primary]
GS114897106950529 [Package]
Contains: 04897106950522
Package: Box [100 Units]
In Commercial Distribution
GS124897106950526 [Package]
Contains: 04897106950522
Package: Carton [1000 Units]
In Commercial Distribution

FDA Product Code

OCXEndoscopic Irrigation/Suction System

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-02
Device Publish Date2020-05-25

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Trademark Results [AquaPulse]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AQUAPULSE
AQUAPULSE
88200334 5878056 Live/Registered
GA HEALTH COMPANY LIMITED
2018-11-20
AQUAPULSE
AQUAPULSE
85291847 4059660 Dead/Cancelled
FINIS Inc.
2011-04-11
AQUAPULSE
AQUAPULSE
78578772 3370245 Dead/Cancelled
Waxman Consumer Products Group Inc.
2005-03-02
AQUAPULSE
AQUAPULSE
74232840 1767363 Dead/Cancelled
SUNBEAM CORPORATION
1991-12-23
AQUAPULSE
AQUAPULSE
73511390 not registered Dead/Abandoned
BRADMILL CASUALWEAR PTY. LTD.
1984-11-30
AQUAPULSE
AQUAPULSE
73310876 1219806 Dead/Cancelled
Location Technology Limited
1981-05-18
AQUAPULSE
AQUAPULSE
73109750 1131711 Dead/Cancelled
APPLIANCE CORPORATION OF AMERICA
1976-12-16
AQUAPULSE
AQUAPULSE
72283295 0876725 Dead/Expired
WESTERN GEOPHYSICAL COMPANY OF AMERICA
1967-10-24
AQUAPULSE
AQUAPULSE
72283294 0884608 Dead/Expired
WESTERN GEOPHYSICAL COMPANY OF AMERICA
1967-10-24

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