Primary Device ID | 06971922131001 |
NIH Device Record Key | b7467c6b-ec31-4ba7-a6f1-badea24e5d4b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VISION TESTER |
Version Model Number | SLY-100 |
Company DUNS | 547954649 |
Company Name | Chongqing Yeasn Science & 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 | false |
Serial Number | false |
Manufacturing Date | false |
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 | 06971922131001 [Primary] |
HKN | Refractor, Manual, Non-Powered, Including Phoropter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-28 |
Device Publish Date | 2020-10-20 |
06971922135030 - YEASN | 2022-08-04 For eye examination and aid in the diagnosis. Contraindications: none. Target groups of patients: adults, children. Intended use |
06971922131070 - YEASN | 2022-04-29 |
06971922131674 - YEASN | 2022-04-29 |
06971922131728 - YEASN | 2022-04-29 |
06971922131926 - YEASN | 2022-04-29 |
06971922132725 - YEASN | 2022-04-29 |
06971922132732 - YEASN | 2022-04-29 |
06971922133029 - YEASN | 2022-04-29 |