HoverJack HJ3902T

GUDID 00816299010435

39" HoverJack

Hovertech International

Manual patient lifting belt/harness
Primary Device ID00816299010435
NIH Device Record Key44f660f4-e51c-4892-9a34-33312bcf3012
Commercial Distribution StatusIn Commercial Distribution
Brand NameHoverJack
Version Model NumberHJ3902T
Catalog NumberHJ3902T
Company DUNS942139841
Company NameHovertech International
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)471-2776
Emailinfo@hovermatt.com
Phone+1(800)471-2776
Emailinfo@hovermatt.com
Phone+1(800)471-2776
Emailinfo@hovermatt.com

Device Dimensions

Width39 Inch
Width39 Inch
Width39 Inch

Operating and Storage Conditions

Storage Environment TemperatureBetween -40 Degrees Fahrenheit and 158 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS100816299010435 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FNGLIFT, PATIENT, AC-POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-07-30

On-Brand Devices [HoverJack]

0081629901043539" HoverJack
0081629901040432" HoverJack

Trademark Results [HoverJack]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HOVERJACK
HOVERJACK
78206388 2949854 Live/Registered
D.T. DAVIS ENTERPRISES, LTD.
2003-01-23

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