| Primary Device ID | 08714729323952 |
| NIH Device Record Key | d9a16447-f167-48aa-95eb-b0d420f121af |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Flexima™ APD™ |
| Version Model Number | M001275070 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| 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 | true |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729323952 [Primary] |
| FFA | TUBE, DRAINAGE, SUPRAPUBIC |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2024-01-03 |
| Device Publish Date | 2016-09-24 |
| 08714729323952 | Drainage Catheter System Kit with Dissolving Tip |
| 08714729323945 | Drainage Catheter System with Dissolving Tip |
| 08714729323136 | Drainage Catheter System |
| 08714729323129 | Drainage Catheter System |
| 08714729323075 | Drainage Catheter System |
| 08714729323068 | Drainage Catheter System |
| 08714729323051 | Drainage Catheter System |
| 08714729271383 | Drainage Catheter System |
| 08714729271376 | Drainage Catheter System |
| 08714729271369 | Drainage Catheter System |
| 08714729191810 | Drainage Catheter System with Dissolving Tip |
| 08714729191803 | Drainage Catheter System with Dissolving Tip |
| 08714729191773 | Drainage Catheter System with Dissolving Tip |
| 08714729191766 | Drainage Catheter System with Dissolving Tip |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FLEXIMA 85498974 5003555 Live/Registered |
B. Braun Medical S.A.S. 2011-12-19 |
![]() FLEXIMA 79062629 not registered Dead/Abandoned |
B. BRAUN MEDICAL SAS 2008-10-08 |
![]() FLEXIMA 78726747 3139010 Live/Registered |
Boston Scientific Scimed, Inc. 2005-10-05 |