Primary Device ID | 16971094537493 |
NIH Device Record Key | 5edcabfb-deab-4f58-8c01-85331cbb7f5d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ceretone |
Version Model Number | CE-A80B |
Company DUNS | 547508199 |
Company Name | Huizhou Jinghao Medical 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 | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06971094537496 [Primary] |
GS1 | 16971094537493 [Package] Contains: 06971094537496 Package: [40 Units] In Commercial Distribution |
QUF | Hearing Aid, Air-Conduction, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-12 |
Device Publish Date | 2023-06-03 |
16971094537493 | CE-A80B |
06971094537489 | CE-A80B |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CERETONE 90403460 not registered Live/Pending |
Ceretone Corp 2020-12-22 |