Primary Device ID | D248137720 |
NIH Device Record Key | 98731825-0f6e-4b25-86e1-5d18d9fd5478 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Almore Aluminum Oxide |
Version Model Number | 13772 |
Company DUNS | 009277971 |
Company Name | HAGER WORLDWIDE, 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 | 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 |