Primary Device ID | 00853455007113 |
NIH Device Record Key | e28f1e6d-c41f-47a3-8f75-0598d6795d8c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | G.LAB |
Version Model Number | MD2200 |
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 | 00853455007113 [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 |