Primary Device ID | 06971094537786 |
NIH Device Record Key | 85630826-7dc2-4053-97cd-fdf1c999dcf7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | METIKO |
Version Model Number | JH-DW2ET |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06971094537786 [Primary] |
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 | 2024-08-26 |
Device Publish Date | 2024-08-18 |
06971094537786 | JH-DW2ET |
16971094537776 | JH-D59CT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
METIKO 90016293 not registered Live/Pending |
Jointown Pharmaceutical Group Co., Ltd. 2020-06-23 |