Primary Device ID | 06936415980702 |
NIH Device Record Key | 8c53c6a6-cf8d-467c-9823-5016dcea0931 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | A3 Anesthesia Delivery System |
Version Model Number | A3 |
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 | 06936415980702 [Primary] |
BSZ | Gas-Machine, Anesthesia |
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 |
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06936415980702 - A3 Anesthesia Delivery System | 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 |