Bethesda Beach Chair Face Mask

GUDID 10840113230461

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

ASPEN SURGICAL PRODUCTS, INC.

Anaesthesia face mask, single-use
Primary Device ID10840113230461
NIH Device Record Keyf7f4ba86-dfc7-462a-9afc-826b241a54c2
Commercial Distribution StatusIn Commercial Distribution
Brand NameBethesda Beach Chair Face Mask
Version Model Number711000
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 Datefalse
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
GS100840113230464 [Primary]
GS110840113230461 [Package]
Contains: 00840113230464
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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