Identity
- Trade Name
- MR PHACO FDA UDI
- Generic Name
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI
- Device Name
- Miyoshi Ultimate Vertical Dual Flow Hydrodissectional Cannula 25ga, Angled 45 Degrees at 1.5mm bend to tip, .2mm Dual Ports set at 120 Degrees, Smooth closed sandblasted tip, 22mm Overall Length FDA UDI
- Model / Reference
- CA1628 FDA UDI
- Description
- Miyoshi Ultimate Vertical Dual Flow Hydrodissectional Cannula 25ga, Angled 45 Degrees at 1.5mm bend to tip, .2mm Dual Ports set at 120 Degrees, Smooth closed sandblasted tip, 22mm Overall Length FDA UDI
Identifiers
- Primary DI / UDI-DI
- G412CA16280 FDA UDI
- FDA Product Code
- HMX FDA UDI
- GMDN Term
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Mr Phaco by Crestpoint Management Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Crestpoint Management Ltd.
Sources (1)
- FDA UDI 7a9d089f-074d-4199-8726-e3840f2903b8 33 fields · synced Jun 1, 2026