Primary Device ID | 00192538901031 |
NIH Device Record Key | 01a87a70-9642-4d4c-b67a-00c4af497786 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Basic Scleral Lens Kit |
Version Model Number | MEN00333 |
Company DUNS | 690680533 |
Company Name | MENICON 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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192538901031 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-11 |
Device Publish Date | 2020-05-01 |
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00192538901079 - Menicon Progent Large Diameter Contact Lens Case | 2021-10-04 |
00192538901017 - Deluxe Scleral Lens Kit | 2020-05-11 |
00192538901024 - Deluxe Kit | 2020-05-11 |
00192538901031 - Basic Scleral Lens Kit | 2020-05-11 |
00192538901031 - Basic Scleral Lens Kit | 2020-05-11 |
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