Primary Device ID | 00075063225127 |
NIH Device Record Key | 5a5c287b-586b-43ce-9c2d-a3ba3cae96a8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Optic Shop |
Version Model Number | 225-12 |
Company DUNS | 002977189 |
Company Name | PROOPTICS LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
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 | 00075063225127 [Primary] |
LRX | Case, Contact Lens |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-05-05 |
00075063225127 | Optic Shop Tight-Top Contact Lens Case 12-Pack |
20075063012509 | Optic Shop Flip-Top Contact Lens Case |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OPTIC SHOP 73118609 1101861 Dead/Expired |
PRO-OPTICS, INC. 1977-03-10 |