Primary Device ID | 00630238122245 |
NIH Device Record Key | 1c9c4a69-791e-48e4-adc9-df4ff1e43508 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 13063 RxSight 0.766x Mag Contact Lens |
Version Model Number | 13063 |
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 | 00630238122245 [Primary] |
GS1 | 00630238122269 [Direct Marking] |
HJK | Lens, Contact, Polymethylmethacrylate, Diagnostic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00630238122245]
Ethylene Oxide
[00630238122245]
Ethylene Oxide
[00630238122245]
Ethylene Oxide
[00630238122245]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-09-19 |
Device Publish Date | 2019-09-11 |
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