| Primary Device ID | 50885403284753 |
| NIH Device Record Key | eaee3b5f-e5f0-45af-9318-499ace6b1e05 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | OTP5000K |
| Catalog Number | OTP5000K |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)323-9088 |
| Customer_Support@BD.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10885403284755 [Primary] |
| GS1 | 50885403284753 [Package] Contains: 10885403284755 Package: Case [10 Units] In Commercial Distribution |
| PXI | Thoracentesis tray |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-15 |
| Device Publish Date | 2018-07-18 |
| 20885403473170 - N/A | 2024-02-27 Surgical Clipper |
| 50885403142176 - Wet Exidine | 2024-02-23 Wet Exidine-4 (CHG 4%) Preoperative Skin Prep Tray |
| 50885403142183 - NA | 2024-02-23 Wet PVP-I Small Procedure Preoperative Skin Prep Tray |
| 50885403142190 - NA | 2024-02-23 Dry Preoperative Skin Prep Tray With Powder-Free Gloves |
| 50885403142220 - NA | 2024-02-23 Dry Surgical Eye Tray |
| 50885403175211 - NA | 2024-02-23 Dry Gauze Preoperative Skin Prep Tray With Powder-Free Gloves |
| 50885403184473 - NA | 2024-02-23 Wet PVP-I Preoperative Skin Prep Tray |
| 50885403184480 - NA | 2024-02-23 Wet PVP-I Vaginal Preoperative Skin Prep Tray |