Primary Device ID | 00817395022926 |
NIH Device Record Key | f8731896-5b49-4787-9b2b-3e7d7789e22a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kennestone Stroke Pack |
Version Model Number | WK440A |
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 |