| Primary Device ID | 10810021178087 |
| NIH Device Record Key | ba88b7b9-ce00-4bd1-9e3e-506a0ebd291d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Goldblatt |
| Version Model Number | HW-F7 |
| Company DUNS | 544332470 |
| Company Name | Dongguan SIMZO Electronic Technology Co., Ltd. |
| Device Count | 1 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 | 00810021178080 [Primary] |
| GS1 | 10810021178087 [Package] Contains: 00810021178080 Package: [1 Units] In Commercial Distribution |
| GS1 | 20810021178091 [Package] Package: [60 Units] In Commercial Distribution |
| FLL | Thermometer, Electronic, Clinical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-06-29 |
| Device Publish Date | 2020-06-20 |
| 18100211780223 | HW-F7 |
| 10810021178087 | HW-F7 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GOLDBLATT 74318325 1814630 Live/Registered |
GREAT STAR TOOLS USA, INC. 1992-09-28 |
![]() GOLDBLATT 72138956 0741950 Dead/Cancelled |
GOLDBLATT TOOL COMPANY 1962-03-02 |
![]() GOLDBLATT 71691853 0620831 Live/Registered |
GOLDBLATT TOOL COMPANY 1955-07-25 |