Primary Device ID | 04544050061209 |
NIH Device Record Key | 2ce85bb6-1292-4426-844a-412b7d9a1051 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SILBRONCHO (LEFT LUNG) |
Version Model Number | #39 |
Catalog Number | 1203539 |
Company DUNS | 715919973 |
Company Name | FUJI SYSTEMS CORPORATION |
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 | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04544050061209 [Primary] |
CBI | Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
04544050061209 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |
04544050061193 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |
04544050061186 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |
04544050061148 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |
14544050123966 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |
14544050123959 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |
14544050123942 | SILBRONCHO Tube is intended for use in airway management of surgical patients to perform one-lun |