| Primary Device ID | 10810011730509 |
| NIH Device Record Key | 50a1b88e-90c9-4206-bd75-07205d37feb4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medhome |
| Version Model Number | IC,30G |
| Company DUNS | 421272490 |
| Company Name | Tianjin Huahong Technology Co., Ltd. |
| Device Count | 310 |
| 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 | 00810011730502 [Primary] |
| GS1 | 10810011730509 [Package] Contains: 00810011730502 Package: case [18600 Units] In Commercial Distribution |
| GS1 | 50810011730507 [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 | 2024-01-24 |
| Device Publish Date | 2024-01-16 |
| 10810011730516 | IC,30G |
| 10810011730509 | IC,30G |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDHOME 97929420 not registered Live/Pending |
CARE FUTURE INC 2023-05-10 |
![]() MEDHOME 97929405 not registered Live/Pending |
CARE FUTURE INC 2023-05-10 |
![]() MEDHOME 85174263 not registered Dead/Abandoned |
PCAS Patient Care Automation Services Inc. 2010-11-11 |