| Primary Device ID | 10810011730554 |
| NIH Device Record Key | 912afa7e-4d7b-4c97-b732-3cc17ceeb549 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BKG |
| Version Model Number | Ordinary Type |
| Company DUNS | 421272490 |
| Company Name | Tianjin Huahong Technology Co., Ltd. |
| Device Count | 100 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810011730557 [Primary] |
| GS1 | 10810011730554 [Package] Contains: 00810011730557 Package: case [5000 Units] In Commercial Distribution |
| GS1 | 50810011730552 [Unit of Use] |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-01 |
| Device Publish Date | 2024-10-24 |
| 10810011730554 - BKG | 2024-11-01 |
| 10810011730554 - BKG | 2024-11-01 |
| 50810011730569 - GLUCORACYIK | 2024-11-01 |
| 10810011730530 - Pro Comfort | 2024-09-03 |
| 10810011730547 - Pro Comfort | 2024-09-03 |
| 10810011730493 - Huahong | 2024-01-24 |
| 10810011730509 - Medhome | 2024-01-24 |
| 10810011730516 - Medhome | 2024-01-24 |
| 50810011730477 - Seren Guard | 2023-11-15 |