| Primary Device ID | 26973069980140 |
| NIH Device Record Key | fd27bd28-15f7-42a5-845d-2274a812cd4e |
| 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 | 10 |
| 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 | 16973069980143 [Primary] |
| GS1 | 26973069980140 [Unit of Use] |
| 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 |