Primary Device ID | 06975683900210 |
NIH Device Record Key | f8d8417b-b6b7-4d97-8d00-6b17ecfd3e9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ou Nuo |
Version Model Number | C100 |
Company DUNS | 723688236 |
Company Name | Changzhou Ou Nuo Medical Equipment 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 | 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 | 06975683900210 [Primary] |
EBH | Material, Impression Tray, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-23 |
Device Publish Date | 2024-08-15 |
06975683900012 | T040RC125N |
06975683900067 | T100RC125N |
06975683900050 | T088RC125N |
06975683900043 | T076RC125N |
06975683900036 | T063RC125N |
06975683900029 | T050RC125N |
06975683900098 | P040 |
06975683900296 | T100 |
06975683900289 | T088 |
06975683900272 | T076 |
06975683900265 | T063 |
06975683900258 | T050 |
06975683900241 | T040 |
06975683900234 | C200 |
06975683900227 | C150 |
06975683900210 | C100 |
06975683900203 | C088 |
06975683900197 | C076 |
06975683900180 | C063 |
06975683900173 | C050 |
06975683900166 | P200 |
06975683900159 | P150 |
06975683900142 | P100 |
06975683900135 | P088 |
06975683900128 | P076 |
06975683900111 | P063 |
06975683900104 | P050 |
06975683900074 | T076MC125N |