Primary Device ID | 00817395021974 |
NIH Device Record Key | 63e0f936-2fb8-4808-b871-86f409705252 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kennestone Angio |
Version Model Number | WK100 |
Company DUNS | 015179820 |
Company Name | PACKROOM LLC |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |