| Primary Device ID | 40616258008507 |
| NIH Device Record Key | c25309bf-98cb-406d-aae0-7effae8678ae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 48” (122 cm) High Pressure Connector Tube |
| Version Model Number | DCT 148 |
| Catalog Number | DCT 148 |
| Company DUNS | 058716649 |
| Company Name | BAYER MEDICAL CARE 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 |
| Phone | +1(800)633-7231 |
| ricustomercomplaints@bayer.com | |
| Phone | +1(800)633-7231 |
| ricustomercomplaints@bayer.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00616258008509 [Primary] |
| GS1 | 20616258008503 [Package] Contains: 00616258008509 Package: [25 Units] In Commercial Distribution |
| GS1 | 40616258008507 [Package] Contains: 20616258008503 Package: [4 Units] In Commercial Distribution |
| DWE | Tubing, Pump, Cardiopulmonary Bypass |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-12-05 |
| 40616258008507 | 48" High Pressure Connector Tube with fixed hub (TUBING, 48" CONNECTOR #82011482, MC) (85029150) |
| 60616258021531 | ASSY,TBG,DCT,48”,MC,WLD (86566761) |