| Primary Device ID | 50810011730569 |
| NIH Device Record Key | 6dfadd49-d120-4759-93e9-6fd4fae3b31a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GLUCORACYIK |
| Version Model Number | IK, 30G |
| Company DUNS | 421272490 |
| Company Name | Tianjin Huahong Technology Co., Ltd. |
| Device Count | 50 |
| 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 | 00810011730564 [Primary] |
| GS1 | 50810011730569 [Unit of Use] |
| QRL | Multiple Use Blood Lancet For Single Patient Use Only |
| 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 |
| 50810011730569 - GLUCORACYIK | 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 |