| Primary Device ID | B160MM361 |
| NIH Device Record Key | db411256-2292-4794-9563-d603bf4bf682 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Procedure Products Lines |
| Version Model Number | MM-36 |
| Company DUNS | 151507563 |
| Company Name | PROCEDURE PRODUCTS, 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 | 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 Issuing Agency | Device ID |
|---|---|
| HIBCC | B160MM361 [Primary] |
| DQO | Catheter, Intravascular, Diagnostic |
| 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 | 2016-12-01 |
| B160P24R1871 | High pressure swivel line, 24" |
| B160P12R1872 | High pressure swivel line |
| B160MM721 | Pressure Line, 72", Male-Male |
| B160MM481 | Pressure Line, 48", male & male |
| B160MM361 | Pressure Line, 36", Male-Male |
| B160MF241 | LINE, MALE/FEMALE-24 IN. |
| B160MF121 | Pressure line, 12", male & female |
| B160MF061 | Pressure Line, 6", male & female |
| B160B72R0722 | High pressure braided swivel line set |
| B160B72F712 | HIGH PRESSURE, 72" BRAIDED LINE |
| B160B48F0711 | Fixed, braided, high-pressure connector |
| B160B36F711 | Fixed, braided, high-pressure connector |
| B160B10R0721 | HIGH PRESSURE BRAIDED SWIVEL LINE, 10" |