Primary Device ID | 16973068560001 |
NIH Device Record Key | efd7db6f-19c0-4970-91ac-b1ba2592f85c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Unifree |
Version Model Number | Y 01 |
Company DUNS | 550904334 |
Company Name | U-Play Products Corporation |
Device Count | 50 |
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 | false |
Manufacturing Date | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973068560004 [Primary] |
GS1 | 16973068560001 [Unit of Use] |
FXX | Mask, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-04 |
Device Publish Date | 2022-10-27 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UNIFREE 90174678 not registered Live/Pending |
U-Play USA LLC 2020-09-11 |
UNIFREE 90064161 not registered Live/Pending |
Li Chunhua 2020-07-21 |
UNIFREE 78130463 not registered Dead/Abandoned |
Rhino Cellular Inc. 2002-05-22 |
UNIFREE 75374094 2271510 Dead/Cancelled |
REDMOND, SCOTT 1997-10-16 |