Primary Device ID | 00859032007088 |
NIH Device Record Key | d05b98d2-d1f7-4d17-895a-898fe6fa331c |
Commercial Distribution Discontinuation | 2025-08-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Panther TPS |
Version Model Number | v5.61 |
Company DUNS | 002162728 |
Company Name | PROWESS, INC. |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |