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Sign in to claim this brandPROCEDURE PRODUCTS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1801 WEST 4TH PLAIN BLVD., Vancouver, WA, 98660
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020778
- DUNS Number
- —
Catalogue (116)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Procedure Products Syringes | 4930-B | FDA UDI | Class II | Active |
| Procedure Products, Inc. | 8039 | FDA UDI | Class II | Unknown |
| Procedure Products Stopcock | 8071F | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4930-Y32 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4930-G21 | FDA UDI | Class II | Active |
| Polycarbonate syringes | 5003-Y | FDA UDI | Class II | Active |
| Procedure Products Needles | 21-1835 | FDA UDI | Class II | Active |
| Procedure Products waste bag | 4822-10 | FDA UDI | Class II | Active |
| Procedure Products Needles | 31-1815 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 5320-Y | FDA UDI | Class II | Active |
| Procedure Products Needle | 31-1845 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 31-1835 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4930-V | FDA UDI | Class II | Active |
| Procedure Products Adapter | 8037 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 9836 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4920-G | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4950-G | FDA UDI | Class II | Active |
| Procedure Products Syringes | 5030-W77 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4930-W87 | FDA UDI | Class II | Active |
| Procedure Products Adapters | 8075 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4410-W | FDA UDI | Class II | Active |
| Procedure Products Needles | 21-1827-P | FDA UDI | Class II | Active |
| Polycarbonate Syringe | 5020-Y | FDA UDI | Class II | Active |
| Polycarbonate Syringe | 5020-Y | FDA UDI | Class II | Active |
| Procedure Products Adapters | 8042 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4930-B43 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4930-Y | FDA UDI | Class II | Active |
| Procedure Products needles | 329-355 | FDA UDI | Class II | Active |
| Procedure Products Needle | 57-0387 | FDA UDI | Class II | Active |
| Procedure Products Needle | 32M-1860 | FDA UDI | Class II | Active |
| Procedure Products Needle | 21-1827 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 5006-G | FDA UDI | Class II | Active |
| Procedure Products Needles | 31-1827-P | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4940-R | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4950-Y | FDA UDI | Class II | Active |
| Procedure Products Syringes | 5003-R | FDA UDI | Class II | Active |
| Procedure Products Catheter Adapter | 8038 | FDA UDI | Class II | Active |
| Procedure Product Torque Device | 8014 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4930-R43 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4930-R | FDA UDI | Class II | Active |
| Procedure Products Syringe | 5370-R | FDA UDI | Class II | Active |
| Procedure Products Needle | 51-1827 | FDA UDI | Class II | Active |
| Procedure Products Line | MF-12LB | FDA UDI | Class II | Active |
| Procedure Products Syringes | 5003-W | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4410-R | FDA UDI | Class II | Active |
| Procedure Products Lines | B72-F071 | FDA UDI | Class II | Active |
| Procedure Products Syringe | 4930-R54 | FDA UDI | Class II | Active |
| Procedure Products Needle | 31-1822 | FDA UDI | Class II | Active |
| Procedure Products Lines | MM-72 | FDA UDI | Class II | Active |
| Procedure Products Syringes | 4410-B | FDA UDI | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 27, 2015 | Z-0355-2016 | — | terminated | The firm had received a complaint alleging that a medical professional had difficulty inserting a guide wire into a needle |