| Primary Device ID | 50885403142176 |
| NIH Device Record Key | 6391488f-f851-47a1-a45f-c7da5ec10845 |
| Commercial Distribution Discontinuation | 2024-03-31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Wet Exidine |
| Version Model Number | 4489 |
| Catalog Number | 4489 |
| Company DUNS | 832696038 |
| Company Name | CAREFUSION 2200, INC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com | |
| Phone | +1(800)523-0502 |
| Customer_Support@BD.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10885403142178 [Primary] |
| GS1 | 50885403142176 [Package] Contains: 10885403142178 Package: Case [20 Units] Discontinued: 2024-03-31 In Commercial Distribution |
| OJU | Skin prep tray |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-02-23 |
| Device Publish Date | 2018-07-18 |
| 10885403075964 - PleurX | 2025-04-25 PLEURX™ PERITONEAL CATHETER MINI KIT |
| 50885403075993 - Denver | 2025-04-25 DENVER™ ASCITES SHUNT DOUBLE-VALVED |
| 50885403076006 - Denver | 2025-04-25 DENVER™ ASCITES SHUNT PERCUTANEOUS ACCESS KIT SINGLE VALVE |
| 50885403076082 - Denver | 2025-04-25 DENVER™ ASCITES SHUNT PERCUTANEOUS ACCESS KIT DOUBLE VALVUE |
| 10885403051722 - V. Mueller | 2024-05-03 LUMBAR AORTOGRAPHY NDL THINWALL 17GA 7IN |
| 10885403049408 - V. Mueller | 2024-05-01 V. Mueller LEFORT URETHRAL SOUND 8FR, THREADED 1/56" FOR STD FILIFORM (NOT INCLUDED) OVERALL LENGTH 11" (28CM) |
| 10885403071263 - V. Mueller | 2024-05-01 V. Mueller CHERRY S-SHAPED BRAIN RETRACTOR 10 AND 13MM WIDE OVERALL LENGTH 6-3/4" (17.1CM) |
| 10885403105159 - V. Mueller | 2024-05-01 V. Mueller CRAIG TOOTHED CUTTER ONLY FOR CRAIG BIOPSY SET OVERALL LENGTH 7-3/8" (18.7CM) |