Primary Device ID | G680LT2061 |
NIH Device Record Key | 4fe35d2c-311d-4120-8b0a-b768eff6cfc2 |
Commercial Distribution Discontinuation | 2025-04-04 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Neocontrol Pelvic Floor Therapy System, Incontinence Treatment Device |
Version Model Number | LT2061 |
Catalog Number | LT2061 |
Company DUNS | 989184851 |
Company Name | BLISSCO MEDICAL DEVICE LIMITED |
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 | false |
OTC Over-The-Counter | true |