Primary Device ID | 10840935102021 |
NIH Device Record Key | 94d2a957-4a9f-41e7-9f33-953bb6a45de4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | All Purpose Cuff |
Version Model Number | 98-0092-10 |
Company DUNS | 148191133 |
Company Name | SUNTECH MEDICAL, 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 | false |
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 | true |
OTC Over-The-Counter | false |