Novasight Hybrid™ PIM
GUDID 00628055603092
Imaging System
Conavi Medical Inc
General-purpose ultrasound imaging system| Primary Device ID | 00628055603092 |
| NIH Device Record Key | c3bd20ed-bba2-426b-8462-9265913e29e6 |
| Commercial Distribution Discontinuation | 2022-11-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Novasight Hybrid™ PIM |
| Version Model Number | TA-07-0002 |
| Company DUNS | 200125243 |
| Company Name | Conavi Medical 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 | false |
| Lot Batch | false |
| 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00628055603092 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K172258
FDA Product Code
| OBJ | Catheter, Ultrasound, Intravascular |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-02 |
| Device Publish Date | 2022-10-25 |
On-Brand Devices [Novasight Hybrid™ PIM]
| 00628055603085 | Imaging System |
| 00628055603092 | Imaging System |
Trademark Results [Novasight Hybrid]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NOVASIGHT HYBRID 88033734 not registered Live/Pending |
Conavi Medical Inc. 2018-07-11 |
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