Primary Device ID | 06936415903527 |
NIH Device Record Key | 335d97aa-004e-48bb-8f79-e4d1bacdd17c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VS-900c Vital Signs Monitor |
Version Model Number | VS-900c |
Company DUNS | 654671304 |
Company Name | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | 06936415903527 [Primary] |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-28 |
Device Publish Date | 2024-11-20 |
06936415985462 - BeneVision N12 OR Patient Monitor | 2024-12-19 |
06936415919283 - uMEC6 Patient Monitor | 2024-12-02 |
06936415903527 - VS-900c Vital Signs Monitor | 2024-11-28 |
06936415903527 - VS-900c Vital Signs Monitor | 2024-11-28 |
06936415980702 - A3 Anesthesia Delivery System | 2024-11-28 |
06944904040301 - VS-900 Vital Signs Monitor | 2024-11-28 |
06944904097923 - cPM 8 Patient Monitor | 2024-11-28 |
06944904097930 - cPM 12 Patient Monitor | 2024-11-28 |
06936415927127 - ePM 12MA Patient Monitor | 2024-11-27 |