Primary Device ID | 00630238107518 |
NIH Device Record Key | 86c6b592-8a07-4f04-ad84-ad132d303943 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Two Mirror Gonio Laser Lens w/ Flange |
Version Model Number | O2MFA |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00630238107518 [Primary] |
GS1 | 00630238107525 [Direct Marking] |
HKS | Prism, Gonioscopic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
[00630238107518]
High-level Disinfectant
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-19 |
Device Publish Date | 2019-06-11 |