Primary Device ID | 20383790002435 |
NIH Device Record Key | f662e4f2-6433-41e0-8542-d06971bef4bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NIPRO BLOOD COLLECTION NEEDLE |
Version Model Number | NM+21G38 |
Catalog Number | NM+21G38-1M |
Company DUNS | 797372554 |
Company Name | NIPRO MEDICAL CORPORATION |
Device Count | 100 |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |
Device Size Text, specify | 0 |
Needle Gauge | 21 Gauge |