DEVICE: Mori Upright Surgical Gonio Lens (00630238101059)
Device Identifier (DI) Information
Mori Upright Surgical Gonio Lens
OMUSG
In Commercial Distribution
OCULAR INSTRUMENTS, INC.
OMUSG
In Commercial Distribution
OCULAR INSTRUMENTS, INC.
No description.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
No | |
No | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
11894 | Gonioscope |
A device intended to be used to examine the angle of the anterior chamber of the eye and for demonstrating ocular motility and rotation.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
HKS | Prism, Gonioscopic |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
9f378a94-499c-4877-a0a1-b700a1debb3f
June 19, 2019
1
June 11, 2019
June 19, 2019
1
June 11, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined