Primary Device ID | 20809160270902 |
NIH Device Record Key | 3673ba81-0adb-4c5a-9adf-c3b3e2ad3d7d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medical Action Industries Inc |
Version Model Number | 81048 |
Company DUNS | 092364462 |
Company Name | MEDICAL ACTION INDUSTRIES INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10809160270905 [Primary] |
GS1 | 20809160270902 [Package] Contains: 10809160270905 Package: [20 Units] In Commercial Distribution |
OJU | Skin prep tray |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-20 |
Device Publish Date | 2019-11-12 |
20809160269845 | 79916 |
20809160270360 | 79817 |
20809160270919 | LH_81045 |
20809160270902 | 81048 |
20809160270896 | 78318 |
20809160270889 | 68549C |
20809160270872 | LH_79893B |
20809160271510 | 79612 |
20809160271756 | 79299B |
20809160271763 | 79950 |