Primary Device ID | 00854924006309 |
NIH Device Record Key | d8d2ab55-3a12-4657-ba18-9d01635b35b9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | C2 CryoBalloon |
Version Model Number | FG-1030 |
Catalog Number | FG-1030 |
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 | 00854924006309 [Primary] |
GEH | Unit, Cryosurgical, Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-09 |
Device Publish Date | 2018-03-08 |
00854924006316 | 180 Standard Catheter 30-mm |
00854924006309 | 90 Standard Catheter 30-mm |
00854924006286 | Focal Standard Catheter 30-mm |
00854924006279 | 180 Pear Catheter |
00854924006262 | 90 Pear Catheter |
00854924006248 | Pear Catheter Focal |
00854924006187 | Foot Pedal |
00854924006170 | Controller |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
C2 CRYOBALLOON 86899206 5177795 Live/Registered |
PENTAX OF AMERICA, INC. 2016-02-05 |