| Primary Device ID | 08714729323112 |
| NIH Device Record Key | 35e57a58-9ae2-458b-af97-f52da473953e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Flexima™ APDL |
| Version Model Number | M001271350 |
| 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 | 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 |
| 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 | 08714729323112 [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 |
| 08714729323976 | Drainage Catheter System Kit with Dissolving Tip |
| 08714729323969 | Drainage Catheter System with Dissolving Tip |
| 08714729323501 | Drainage Catheter System Kit |
| 08714729323495 | Drainage Catheter System Kit |
| 08714729323488 | Drainage Catheter System Kit |
| 08714729323471 | Drainage Catheter System Kit |
| 08714729323150 | Drainage Catheter System |
| 08714729323143 | Drainage Catheter System |
| 08714729323112 | Drainage Catheter System |
| 08714729323105 | Drainage Catheter System |
| 08714729323099 | Drainage Catheter System |
| 08714729323082 | Drainage Catheter System |
| 08714729323044 | Drainage Catheter System |
| 08714729300694 | Drainage Catheter System Kit |
| 08714729300670 | Drainage Catheter System |
| 08714729191827 | Drainage Catheter System with Dissolving Tip |
| 08714729191797 | Drainage Catheter System with Dissolving Tip |
| 08714729191780 | Drainage Catheter System with Dissolving Tip |
| 08714729191759 | Drainage Catheter System |
| 08714729127970 | 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 |