| Primary Device ID | 00854924006248 |
| NIH Device Record Key | 4e8a4c09-4552-49c9-84de-71b0a2c0f4e5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | C2 CryoBalloon |
| Version Model Number | FG-1024 |
| Catalog Number | FG-1024 |
| 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 | 00854924006248 [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 | 2018-04-26 |
| Device Publish Date | 2018-03-26 |
| 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 |