| Primary Device ID | 10383790001318 |
| NIH Device Record Key | 3647d3ea-74f8-445e-9349-6059accfc4c7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER |
| Version Model Number | 16GX1" HC-30W-D-CAP |
| Catalog Number | FD+162530BC-CAP |
| Company DUNS | 797372554 |
| Company Name | NIPRO MEDICAL CORPORATION |
| 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 |
| 40383790003320 | DULL FISTULA NEEDLE
for Established Access Sites Only
16Gx1" Fixed Hub 16" Tubing |
| 40383790003313 | DULL FISTULA NEEDLE
for Established Access Sites Only
15Gx1" Fixed Hub 16" Tubing |
| 40383790001388 | DULL FISTULA NEEDLE for Established Access Sites Only
17Gx1" Fixed Hub 12" Tubing |
| 40383790001326 | DULL FISTULA NEEDLE for Established Access Sites Only
16Gx1" Rotating Hub 12" Tubing |
| 10383790001318 | DULL FISTULA NEEDLE for Established Access Sites Only
16Gx1" Fixed Hub 12" Tubing |
| 10383790001288 | DULL FISTULA NEEDLE for Established Access Sites Only
15Gx1-1/4" Rotating Hub 12" Tubing |
| 40383790001272 | DULL FISTULA NEEDLE for Established Access Sites Only
15Gx1-1/4" Fixed Hub 12" Tubing |
| 40383790001258 | DULL FISTULA NEEDLE for Established Access Sites Only
15Gx1" Rotating Hub 12" Tubing |
| 40383790001241 | DULL FISTULA NEEDLE for Established Access Sites Only
15Gx1" Fixed Hub 12" Tubing |
| 10383790001189 | DULL FISTULA NEEDLE for Established Access Sites Only
14Gx1" Fixed Hub 12" Tubing |