Primary Device ID | 00636266957262 |
NIH Device Record Key | 7e9b78b7-d810-4587-8a3e-cdb44903265e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SONUS V SCALER |
Version Model Number | Sonus V |
Catalog Number | A52000 |
Company DUNS | 002965168 |
Company Name | ENGLER ENGINEERING CORPORATION |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00636266957262 [Primary] |
ELC | Scaler, 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 | 2018-08-16 |
Device Publish Date | 2018-07-16 |
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