Primary Device ID | 06923509303004 |
NIH Device Record Key | 096db21d-9253-450d-aa91-d4d3a4ffb6af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CASOFT |
Version Model Number | 60*90 |
Company DUNS | 679723387 |
Company Name | Fujian Putian Licheng Paper Industry Co.,Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Serial Number | false |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06923509303004 [Primary] |
KME | Bedding, Disposable, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-01 |
Device Publish Date | 2023-02-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CASOFT 98107466 not registered Live/Pending |
Chongqing Huanyu Technology Co., Ltd. 2023-07-28 |