Primary Device ID | 00857863007338 |
NIH Device Record Key | cd370220-8dc2-4c71-adf3-9d5676727def |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aero/Vent Jr. |
Version Model Number | AV-101A |
Company DUNS | 079628327 |
Company Name | Medi/Nuclear Corporation, 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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800-321-5981 |
cs@medinuclear.com |
Special Storage Condition, Specify | Between 0 and 0 *store at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857863007338 [Primary] |
IYT | System, Rebreathing, Radionuclide |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-06-09 |
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