Primary Device ID | 00841517104030 |
NIH Device Record Key | 10807c39-1852-4125-8f42-61181a6070d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | P21v/5-1 MHz |
Version Model Number | P18800-50 |
Catalog Number | P18800 |
Company DUNS | 014438860 |
Company Name | FUJIFILM SONOSITE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
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 |
Phone | +1(999)999-9999 |
xx@xx.xx |
Handling Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841517104030 [Primary] |
ITX | Transducer, ultrasonic, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-31 |
Device Publish Date | 2019-07-23 |
00841517104030 | Diagnostic Ultrasound Transducer |
00841517104023 | Diagnostic Ultrasound Transducer |
00841517103958 | Diagnostic Ultrasound Transducer |
00841517101992 | Diagnostic Ultrasound Transducer |
00841517101893 | Diagnostic Ultrasound Transducer |
00841517101428 | Diagnostic Ultrasound Transducer |
00841517105181 | P18800-51 |
00841517106676 | Diagnostic Ultrasound Transducer |
00841517107222 | P26081-02 |
00841517108564 | Diagnostic Ultrasound Transducer |