MR Phaco CA469
MR Phaco CA469 is a Class I device made by Crestpoint Management Ltd., listed in FDA GUDID since 30 May 2025 (UDI-DI G412CA4690), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberG412CA4690 | Date30 May 2025 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MR Phaco
- Generic name
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
- Model / reference
- CA469
- Primary DI / UDI-DI
- G412CA4690
- FDA product code
- HMX
- GMDN term
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable.
- Stephens Instruments SC-1565 by KRISHNA IMPORTS INC
- Stephens Instruments SC-1475 by KRISHNA IMPORTS INC
- LAMINAR OPOS19L by Johnson & Johnson Surgical Vision, Inc.
- Eckardt Backflush Handpiece with luer lock.(23 gauge / 0.6 mm) 1281.C by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
- LAMINAR OPOS20L by Johnson & Johnson Surgical Vision, Inc.
- Cannula 8-601-2 by Duckworth & Kent Ltd.
- I/A Tip 8-731-1 by Duckworth & Kent Ltd.
- Anterior Chamber Maintainer 2520 by Hurricane Medical
- Replacement backflush Needle, straight.(23 gauge / 0.6 mm) 1281.A506 by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.