WIPEABLE GAIT BELT 54 INCH W/ PLASTIC BUCKLE BLUE

GUDID 00733657216134

ALIMED, INC.

Movement-resistance gait rehabilitation device
Primary Device ID00733657216134
NIH Device Record Key94aeff4d-b7e2-4db9-87cc-c25b6c3457e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameWIPEABLE GAIT BELT 54 INCH W/ PLASTIC BUCKLE BLUE
Version Model Number711026
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
GS100733657216134 [Primary]

FDA Product Code

IKXAID, TRANSFER

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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00733657230253 - CUSH DROP AWAY POMMEL 16X162024-02-19
00733657230260 - DROP AWAY POMMEL CUSHION 18X162024-02-19
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