BARIATRIC BED WEDGE (26Wx25Lx8H)

GUDID 00733657194203

ALIMED, INC.

Freestanding patient positioner, reusable
Primary Device ID00733657194203
NIH Device Record Keyaa24e116-525d-4b08-a38e-5dc499f2172e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBARIATRIC BED WEDGE (26Wx25Lx8H)
Version Model Number82956
Company DUNS056007248
Company NameALIMED, INC.
Device Count1
DM Exempttrue
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 Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com
Phone+1(781)329-2900
Emailcustomerservice@alimed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100733657194203 [Primary]

FDA Product Code

FMPProtector, skin pressure

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-09
Device Publish Date2022-12-01

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