| Primary Device ID | 08806383562485 |
| NIH Device Record Key | 0a9e3d5d-c994-4c45-856c-f8f7d2b55d71 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Irrigation Tip |
| Version Model Number | END OPEN TYPE 20G |
| Catalog Number | 951-203 |
| Company DUNS | 687789453 |
| Company Name | DiaDent Group International |
| 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 | false |
| Lot Batch | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08806383562485 [Primary] |
| JEW | Tip, Rubber, Oral Hygiene |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-02 |
| Device Publish Date | 2020-08-25 |
| 08806383562515 | This device connected with manually-operated syringe only is used in order to spray oral cavity |
| 08806383562508 | This device connected with manually-operated syringe only is used in order to spray oral cavity |
| 08806383562492 | This device connected with manually-operated syringe only is used in order to spray oral cavity |
| 08806383562485 | This device connected with manually-operated syringe only is used in order to spray oral cavity |
| 08806383562478 | This device connected with manually-operated syringe only is used in order to spray oral cavity |
| 08806383562461 | This device connected with manually-operated syringe only is used in order to spray oral cavity |