KXL System 110-02723
by Avedro, Inc. United States GUDID
Product code HMF
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00855574003007 | Date2 Jan 2019 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- KXL System
- Generic Name
- Ophthalmic crosslinking ultraviolet phototherapy system
- Model / Reference
- 110-02723
- Primary DI / UDI-DI
- 00855574003007
- FDA Product Code
- HMF
- GMDN Term
- Ophthalmic crosslinking ultraviolet phototherapy system
- Device Class
- Class I
- Regulation Number
- 886.1860
- Commercial Distribution
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Other devices from Avedro, Inc.
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 41a977d3-664b-400e-88ce-3db9a7aaf683