Primary Device ID | 06973509180006 |
NIH Device Record Key | b3cd0ceb-b5f6-4b00-82b8-f1c311680fca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tongda |
Version Model Number | 17.5X9.5cm |
Company DUNS | 547247122 |
Company Name | Xiantao Tongda Non-Woven Products 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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 | 06973509180006 [Primary] |
QKR | Face Mask Per Enforcement Policy For Face Masks And Respirators During The Declared Public Health Emergency |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-12 |
Device Publish Date | 2022-12-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TONGDA 86001714 4566730 Live/Registered |
ZHENGZHOU DANDIAN TECHNOLOGY SOFTWARE LTD. 2013-07-03 |
TONGDA 79066053 3870236 Live/Registered |
Beijing Tongd Refractory Technologies Co., Ltd. 2008-11-11 |