| Primary Device ID | 00630238007351 |
| NIH Device Record Key | 19dd0e87-be6a-4dde-9a45-2fe408f63e8f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Peyman G. Capsulotomy Yag Laser Lens |
| Version Model Number | OPYG-12-12 |
| Company DUNS | 046212387 |
| Company Name | OCULAR INSTRUMENTS, INC. |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00630238007351 [Primary] |
| GS1 | 00630238020053 [Direct Marking] |
| HJK | Lens, Contact, Polymethylmethacrylate, Diagnostic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
[00630238007351]
High-level Disinfectant
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-12-09 |