Primary Device ID | 06944904088167 |
NIH Device Record Key | 129b9447-2956-4ad7-be28-08d99748e9c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | P7-3TE Ultrasonic Probe(FDA) |
Version Model Number | 120-002202-00 |
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 | true |
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 |