Primary Device ID | 06936415925635 |
NIH Device Record Key | 9ae59b32-d0b5-4726-bc4b-d45e2dd09e39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DC-80A Pro Diagnostic Ultrasound System |
Version Model Number | DC-80A Pro |
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 | 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 | 06936415925635 [Primary] |
IYN | System, Imaging, Pulsed Doppler, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-26 |
Device Publish Date | 2025-02-18 |
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