AFO CHILD LEFT

GUDID 00656204005053

ALIMED, INC.

Ankle/foot orthosis
Primary Device ID00656204005053
NIH Device Record Key66460f5e-104a-4273-86fc-e3b4e3c0783e
Commercial Distribution StatusIn Commercial Distribution
Brand NameAFO CHILD LEFT
Version Model Number66132/NA/LM
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
GS100656204005053 [Primary]

FDA Product Code

ITWJOINT, ANKLE, EXTERNAL BRACE

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

On-Brand Devices [AFO CHILD LEFT]

0065620400511466132/NA/LXS
0065620400509166132/NA/LXL
0065620400507766132/NA/LS
0065620400505366132/NA/LM
0065620400494066132/NA/LL

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