Primary Device ID | 06970953260063 |
NIH Device Record Key | 1e753f94-a2b7-4756-bd98-4f4771d19a30 |
Commercial Distribution Discontinuation | 2019-05-15 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fitfaith |
Version Model Number | M130E |
Company DUNS | 544436982 |
Company Name | Shenzhen Fitfaith Technology Co., Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
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 |