Primary Device ID | 00841517101879 |
NIH Device Record Key | c31a0aac-ef8a-4445-8129-fdfa1c366d1a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | L38v/10-5 MHz |
Version Model Number | P19360-18 |
Catalog Number | P19360 |
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 |
xyz@xyz.com |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841517101879 [Primary] |
ITX | Transducer, ultrasonic, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-05-23 |
Device Publish Date | 2017-02-20 |
00841517104047 | Diagnostic Ultrasound Transducer |
00841517102005 | Diagnostic Ultrasound Transducer |
00841517101879 | Diagnostic Ultrasound Transducer |
00841517101435 | Diagnostic Ultrasound Transducer |
00841517100889 | Diagnostic Ultrasound Transducer |
00841517105662 | P19360-15A |
00841517105174 | P19360-51 |
00841517106683 | Diagnostic Ultrasound Transducer |
00841517107215 | P26082-02 |
00841517108571 | Diagnostic Ultrasound Transducer |