Duns Number:690635461
Device Description: This combination delivery unit is need to comprise the combination system which enables ra This combination delivery unit is need to comprise the combination system which enables radiation of the red, yellow, or green laser beam or YAG laser beam while performing the observation with the slit lamp of the YAG laser system. This delivery unit is mounted on the slit lamp of the YAG laser system and connected to the NIDEK Multicolor Laser Photocoagulator MC-500 using the MC connecting cable and fiber optic cable. The combination system allows selection between photocoagulation with the red (647 nm), yellow (577 nm), or green (532 nm) laser beam and YAG laser beam (wavelength: 1064 nm (pulse laser)). In addition, they are selected easily by changing the optical path of the laser beam with the laser selectlever, and various kinds of safety devices are integrated into the system to make sure that only the selected laser beam is radiated. This combination delivery unit is the only delivery unit that can be connected both to the NIDEK Multicolor Laser Photocoagulator MC-500 and the NIDEK Ophthalmic YAG Laser System YC-1800.
Catalog Number
-
Brand Name
YAG laser combination delivery unit (YC-1800)
Version/Model Number
17367-0000
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
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Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
HQF
Product Code Name
Laser, Ophthalmic
Public Device Record Key
600424b0-4ea8-4e6f-bc5b-26d31469c64f
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
February 01, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 39 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 73 |
| 3 | A medical device with high risk that requires premarket approval | 5 |