Primary Device ID | 00841517104870 |
NIH Device Record Key | 55cf5b22-675b-433b-897b-be4d5d2f1452 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | L38xi/10-5 MHz |
Version Model Number | P19626-20 |
Catalog Number | P19626 |
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 |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841517104870 [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 | 2019-08-01 |
Device Publish Date | 2019-07-24 |
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