HARNESS PAVLIK TYPE

GUDID 00656204000225

ALIMED, INC.

Infant hip harness
Primary Device ID00656204000225
NIH Device Record Key526a22fe-ed71-4bac-8af3-a3aca187333a
Commercial Distribution StatusIn Commercial Distribution
Brand NameHARNESS PAVLIK TYPE
Version Model Number51968/NA/SM
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
GS100656204000225 [Primary]

FDA Product Code

IQZHAND, EXTERNAL LIMB COMPONENT, POWERED

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 [HARNESS PAVLIK TYPE]

0065620400614251968/NA/XS
0065620400023251968/NA/XL
0065620400022551968/NA/SM
0065620400021851968/NA/MD
0065620400020151968/NA/LG

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