Primary Device ID | 20809160194734 |
NIH Device Record Key | a4866de8-7489-4397-8bae-6cb4f51e0c2b |
Commercial Distribution Discontinuation | 2019-04-03 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | AVIDTruCustom |
Version Model Number | VAMM036-05 |
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 | false |
OTC Over-The-Counter | true |
Special Storage Condition, Specify | Between 0 and 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10809160194737 [Primary] |
GS1 | 20809160194734 [Package] Contains: 10809160194737 Package: [20 Units] Discontinued: 2019-04-03 Not in Commercial Distribution |
NSB | Patient personal hygiene kit |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-04-04 |
Device Publish Date | 2018-05-17 |
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