Manual Bed FL23SM

GUDID 26704820000032

Manual Med/Surg articulated bed.

Umano Medical Inc

Manual hospital bed
Primary Device ID26704820000032
NIH Device Record Keyb9ed9525-6ecc-4c22-9052-7e5ba26e365d
Commercial Distribution Discontinuation2016-09-21
Commercial Distribution StatusNot in Commercial Distribution
Brand NameManual Bed
Version Model NumberFL23SM
Catalog NumberFL23SM
Company DUNS249675476
Company NameUmano Medical Inc
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
GS116704820000035 [Primary]
GS126704820000032 [Package]
Contains: 16704820000035
Package: [1 Units]
Discontinued: 2016-09-21
Not in Commercial Distribution
GS136704820000039 [Package]
Contains: 16704820000035
Package: [2 Units]
Discontinued: 2016-09-21
Not in Commercial Distribution

FDA Product Code

FNJBed, Manual

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 Date2016-11-30

On-Brand Devices [Manual Bed]

20670482000030Manual Med/Surg articulated bed.
26704820000032Manual Med/Surg articulated bed.

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