Primary Device ID | 00087701434297 |
NIH Device Record Key | 42445bbf-c3f3-4a18-9289-3a9686b5cc37 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GNP |
Version Model Number | 09562GNP |
Company DUNS | 007914906 |
Company Name | AMERISOURCEBERGEN DRUG 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 | false |
OTC Over-The-Counter | false |