Primary Device ID | 10840935102229 |
NIH Device Record Key | 10737a36-88da-4a8f-8c84-66220e95e186 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | All Purpose Cuff |
Version Model Number | 98-0099-04 |
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 |