Primary Device ID | B390WB9903111 |
NIH Device Record Key | e91fe281-31b4-44a7-86e8-09d734ce6257 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reprocessed Celon ProSleep Plus RFITT, 1.3mm, 0-25W, 2 Pins. |
Version Model Number | WB990311 |
Company DUNS | 785616934 |
Company Name | SURETEK MEDICAL |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |