Jessie Arm Suspension Kit

GUDID 10840113230676

Intended to support and maintain the position of an anesthetized patient during surgery

ASPEN SURGICAL PRODUCTS, INC.

Arm procedure positioner, single-use
Primary Device ID10840113230676
NIH Device Record Key71d0513c-1238-41a8-a459-c78652e298ef
Commercial Distribution StatusIn Commercial Distribution
Brand NameJessie Arm Suspension Kit
Version Model Number711300
Company DUNS027680821
Company NameASPEN SURGICAL PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840113230679 [Primary]
GS110840113230676 [Package]
Contains: 00840113230679
Package: [10 Units]
In Commercial Distribution

FDA Product Code

CCXSUPPORT, PATIENT POSITION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-30
Device Publish Date2021-03-22

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