Beds by George

GUDID 05060493790036

36x80

BEDS BY GEORGE

Basic electric hospital bed
Primary Device ID05060493790036
NIH Device Record Keyaa7f364b-4941-48cd-9751-483901a3f576
Commercial Distribution StatusIn Commercial Distribution
Brand NameBeds by George
Version Model Number190
Company DUNS054233501
Company NameBEDS BY GEORGE
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS105060493790036 [Primary]

FDA Product Code

FNLBed, Ac-Powered Adjustable Hospital

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-19

On-Brand Devices [Beds by George]

0506049379011136x80 semi-electric
0506049379010436x80 semi-electric
0506049379009836x80 semi-electric
0506049379008136x80 semi-electric
0506049379007436x80
0506049379006736x76
0506049379005036x80
0506049379004336x76
0506049379003636x80
0506049379002936x76
0506049379001236x80
0506049379000536x76

Trademark Results [Beds by George]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BEDS BY GEORGE
BEDS BY GEORGE
77390014 3504446 Live/Registered
Beds By George, Inc.
2008-02-06

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.