| Primary Device ID | 06973069980146 | 
| NIH Device Record Key | d65796e8-5651-488e-a29f-965e83e516b7 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | APPLICATOR | 
| Version Model Number | NA | 
| Company DUNS | 529882730 | 
| Company Name | Dalian Rongbang Medical Devices Co.,Ltd. | 
| Device Count | 1 | 
| DM Exempt | true | 
| 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 | false | 
| 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 | 06973069980146 [Primary] | 
| KCJ | Applicator, Ent | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2022-09-15 | 
| Device Publish Date | 2022-09-07 | 
| 26973069980140 | NA | 
| 06973069980146 | NA | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  APPLICATOR  77502937  3567408 Live/Registered | Sealant, Waterproofing & Restoration Institute 2008-06-19 | 
|  APPLICATOR  76034720  2667681 Live/Registered | Endress + Hauser Flowtec AG 2000-04-25 |