| Primary Device ID | 16971919460494 |
| NIH Device Record Key | ac66db25-a6d9-4ab8-90b2-b343cdcc730e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medi Grade |
| Version Model Number | 90ml |
| Company DUNS | 543014978 |
| Company Name | Ningbo Albert Novosino 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 | false |
| 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 | 16971919460494 [Primary] |
| KCP | Syringe, Ent |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-11-25 |
| Device Publish Date | 2025-11-17 |
| 16971919460432 | 75ml |
| 16971919460494 | Ear bulb Syringe kit |
| 16971919460449 | nasal rinse bottle |
| 16971919460500 | Earwax removal Syringe |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDI GRADE 88876606 not registered Live/Pending |
FBGC Limited 2020-04-17 |
![]() MEDI GRADE 73707496 1521063 Dead/Cancelled |
INTERFACE, INC. 1988-01-25 |