ROLLER FOAM FULL ROLL 36" LONG X 6" WIDE ALIMED 3/CS

GUDID 00662641648524

ALIMED, INC.

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Primary Device ID00662641648524
NIH Device Record Keyb9c53d23-0458-4730-b243-a7049bdc1172
Commercial Distribution StatusIn Commercial Distribution
Brand NameROLLER FOAM FULL ROLL 36" LONG X 6" WIDE ALIMED 3/CS
Version Model Number3171603
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100662641648524 [Primary]

FDA Product Code

IONEXERCISER, NON-MEASURING

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 [ROLLER FOAM FULL ROLL 36" LONG X 6" WIDE ALIMED 3/CS]

006626416485243171603
007336572906843171603

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