Primary Device ID | 00817136025216 |
NIH Device Record Key | ef81d62c-5ca8-44d9-956b-0e3aeb6dc392 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 5510 7L SYRINGE |
Version Model Number | 5510 |
Catalog Number | CR1396 |
Company DUNS | 007131725 |
Company Name | HANS RUDOLPH, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 |