Mydcombi FG-16427
by Eyenovia, Inc. GUDID
Withdrawn
Overview
A reusable non-sterile component of the MydCombi drug delivery system. Working in conjunction with the Cartridge, this base contains the drive system that allows actuation of the mist. It also contains the power source and interfaces with an external charging source.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00860009909700 | Date14 Jun 2023 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- Mydcombi
- Generic Name
- Battery box
- Model / Reference
- FG-16427
- Primary DI / UDI-DI
- 00860009909700
- FDA Product Code
- KYX
- GMDN Term
- Battery box
- Device Class
- Class I
- Regulation Number
- 880.6430
- Commercial Distribution
- Not in Commercial Distribution
Properties
Other properties (8)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- HCT/P: No
- Serial Number: No