Primary Device ID | 00854924006163 |
NIH Device Record Key | 833f1e22-2974-4508-a099-0b95779b95e1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BOA Endoscopic Valve |
Version Model Number | FG-1016 |
Catalog Number | FG-1016 |
Company DUNS | 929139249 |
Company Name | C2 THERAPEUTICS, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00854924006163 [Primary] |
OCX | Endoscopic Irrigation/Suction System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-10-19 |
00854924006118 - Sidecar External Working Channel | 2018-07-06 Sidecar External Working Channel, Endoscopic Accessory |
00854924006163 - BOA Endoscopic Valve | 2018-07-06BOA Endoscopic Valve, Endoscopic Accessory |
00854924006163 - BOA Endoscopic Valve | 2018-07-06 BOA Endoscopic Valve, Endoscopic Accessory |
00854924006170 - C2 CryoBalloon | 2018-07-06 Controller |
00854924006187 - C2 CryoBalloon | 2018-07-06 Foot Pedal |
00854924006323 - C2 CryoBalloon Full 8 Catheter | 2018-07-06 C2 CryoBalloon Full 8 Catheter for C2 CryoBalloon Ablation System |
00854924006330 - C2 CryoBalloon Focal Pear Catheter | 2018-07-06 C2 CryoBalloon Focal Pear Catheter for C2 CryoBalloon Ablation System |
00854924006248 - C2 CryoBalloon | 2018-04-26 Pear Catheter Focal |
00854924006262 - C2 CryoBalloon | 2018-04-26 90 Pear Catheter |