Primary Device ID | 06973576425444 |
NIH Device Record Key | d414eb8a-f080-4933-9556-9baf544480a3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ruyue |
Version Model Number | 10 |
Company DUNS | 554529787 |
Company Name | Shandong Ruyue Medical Technology Co.,Ltd |
Device Count | 1000 |
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 | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 06973576425437 [Primary] |
GS1 | 06973576425444 [Unit of Use] |
FMC | Patient Examination Glove |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-17 |
Device Publish Date | 2024-06-07 |
06973576425444 | 10 |
06973576425338 | 10 |
06973576425215 | 10 |
06973576425000 | 20 |
06973576425550 | 12 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RUYUE 87943532 5654983 Live/Registered |
Sun, Qixue 2018-05-31 |