Primary Device ID | 00810014760605 |
NIH Device Record Key | 7b918bf9-123d-4d9c-aa6e-7313ae429d88 |
Commercial Distribution Discontinuation | 2020-03-25 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Safe Warrior |
Version Model Number | MSK1001 |
Company DUNS | 008408527 |
Company Name | REALHER PRODUCTS INC. |
Device Count | 20 |
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 | true |
Lot Batch | true |
Serial Number | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810014760605 [Primary] |
GS1 | 00810014760803 [Unit of Use] |
GS1 | 00810014760810 [Package] Package: CASE [110 Units] Discontinued: 2020-03-25 Not in Commercial Distribution |
FXX | Mask, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2020-03-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SAFE WARRIOR 88845059 not registered Live/Pending |
REALHER PRODUCTS INC. 2020-03-24 |