Primary Device ID | 00860010778609 |
NIH Device Record Key | 9eeb9501-9660-4c20-88b9-c946798bb290 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Amron Oxygen Treatment Hood |
Version Model Number | 8891-03S |
Company DUNS | 086003852 |
Company Name | Amron International, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com | |
Phone | 17602086500 |
scott@amronintl.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860010778609 [Primary] |
FOG | Hood, Oxygen, Infant |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-18 |
Device Publish Date | 2023-08-10 |