Primary Device ID | 00630238107679 |
NIH Device Record Key | 048775f6-fb40-425b-bb94-aa2faf39a46d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 2.0mm Fundus Laser Lens |
Version Model Number | OFA2.0 |
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 | 00630238077026 [Direct Marking] |
GS1 | 00630238107679 [Primary] |
HJK | Lens, Contact, Polymethylmethacrylate, Diagnostic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
[00630238107679]
High-level Disinfectant
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-18 |
Device Publish Date | 2019-06-10 |