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 |