| Primary Device ID | 10801741086103 |
| NIH Device Record Key | cc28351a-7826-4cc8-a563-416c76e75473 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENCOR ENSPIRE® |
| Version Model Number | DS4002 |
| Catalog Number | DS4002 |
| Company DUNS | 043674543 |
| Company Name | SENORX, 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)321-4254 |
| medical.services@crbard.com | |
| Phone | +1(800)321-4254 |
| medical.services@crbard.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741086106 [Primary] |
| GS1 | 10801741086103 [Package] Contains: 00801741086106 Package: CA [12 Units] In Commercial Distribution |
| KNW | INSTRUMENT, BIOPSY |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-20 |
| 00801741086113 | ENCOR ENSPIRE® Breast Biopsy System |
| 10801741086103 | ENCOR ENSPIRE® Breast Biopsy System Vacuum Tubing Cassette |
| 10801741086097 | ENCOR ENSPIRE® Breast Biopsy System Vacuum and Rinse Tubing Cassette |
| 00801741085956 | ENCOR ENSPIRE® Breast Biopsy System Driver Holder |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ENCOR ENSPIRE 85231385 4168792 Live/Registered |
C. R. Bard, Inc. 2011-02-01 |