Primary Device ID | 06976198710486 |
NIH Device Record Key | a9c78fe6-4c2b-4e8c-a4a9-ec45aed52c0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | YINKANG |
Version Model Number | YKB004-3 |
Company DUNS | 544339169 |
Company Name | Hubei Yinkang Medical Equipment 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 | false |
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 | 06976198710486 [Primary] |
FNJ | Bed, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-10 |
Device Publish Date | 2023-03-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() YINKANG 97821686 not registered Live/Pending |
Shenzhen Kanglifa Technology Co., Ltd. 2023-03-03 |