| Primary Device ID | 00853821006023 |
| NIH Device Record Key | 018e033f-978b-4222-ad4f-0268fb598408 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GoWISE USA |
| Version Model Number | GW22025 |
| Company DUNS | 005175432 |
| Company Name | MING'S MARK INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 | 00853821006023 [Primary] |
| GS1 | 10853821006020 [Package] Package: Case [1 Units] In Commercial Distribution |
| GS1 | 20853821006027 [Package] Contains: 10853821006020 Package: Pallet [4 Units] In Commercial Distribution |
| FRI | Scale, Stand-On, Patient |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-08-23 |