Amron Oxygen Treatment Hood

GUDID 00860010778609

02 VINYL HOOD W/OPTICAL WINDOW, NECK RING ASSEMBLY, STRAPS AND UNTRIMMED SILICONE NECK SEAL

Amron International, Inc.

Oxygen administration hood, adult
Primary Device ID00860010778609
NIH Device Record Key9eeb9501-9660-4c20-88b9-c946798bb290
Commercial Distribution StatusIn Commercial Distribution
Brand NameAmron Oxygen Treatment Hood
Version Model Number8891-03S
Company DUNS086003852
Company NameAmron International, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
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

Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com
Phone17602086500
Emailscott@amronintl.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860010778609 [Primary]

FDA Product Code

FOGHood, Oxygen, Infant

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-18
Device Publish Date2023-08-10

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