Primary Device ID | 05060981240005 |
NIH Device Record Key | 51deb67a-c696-47fe-9d7d-c36f68d5659a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KINEON |
Version Model Number | XG-01B |
Company DUNS | 543062382 |
Company Name | Shenzhen Kaiyan 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 | true |
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 | 05060981240005 [Primary] |
ILY | Lamp, Infrared, Therapeutic Heating |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-03 |
Device Publish Date | 2023-07-26 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() KINEON 97615962 not registered Live/Pending |
Reviiv Light LLC 2022-10-01 |