Primary Device ID | 00816787020397 |
NIH Device Record Key | 7b1b68d4-82fd-413b-96a8-b3c3c3de6a5c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 812 FOREIGN 220V SALES KIT |
Version Model Number | 812 (F) 220V |
Company DUNS | 009041773 |
Company Name | PARKS MEDICAL ELECTRONICS, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |