Primary Device ID | 06936415912604 |
NIH Device Record Key | cb6e1904-e070-4ce2-8aa9-467109d52e64 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RM Module(package/no accessory) |
Version Model Number | 115-034114-00 |
Company DUNS | 654671304 |
Company Name | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +8675581888998 |
service@mindray.com.cn |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06936415912604 [Primary] |
BZQ | Monitor, Breathing Frequency |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-08 |
Device Publish Date | 2020-04-30 |
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