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 |