| Primary Device ID | 00853455007144 |
| NIH Device Record Key | dc6da82a-ae70-4034-b6e4-0b71e0cd0ecc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | G.LAB |
| Version Model Number | MD1180 |
| Company DUNS | 058430522 |
| Company Name | ACESO HEALTHCARE PRODUCTS, INC. |
| 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 | false |
| 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 | 00853455007144 [Primary] |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-21 |
| Device Publish Date | 2019-11-13 |
| 00853455007083 | PR0200 |
| 00853455007076 | PR0100 |
| 00853455007007 | MD4180 |
| 00853455007151 | MD2222 |
| 00853455007144 | MD1180 |
| 00853455007113 | MD2200 |
| 00853455007106 | MD41W1 |
| 00853455007090 | MD41W0 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() G.LAB 86920608 5121082 Live/Registered |
CHOW, Lai Yu 2016-02-26 |