gudid
Primary ID: PH85112
MR PHACO (UDI PH85112)
Manufactured by Crestpoint Management Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MR PHACO - Primary ID PH85112
Device Regulatory Overview
The MR PHACO (Model/Catalog Number: PH85112) is a medical device manufactured by Crestpoint Management Limited. This product is indexed under FDA Product Code / Category Classification HMX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PH85112
- Product Code / EMDN
- HMX
- Device Name
- I/A Silicone Straight Tip ONLY, Silicone Outer Sleeve, 19ga Closed Inner Cannula tip with .5mm Aspirating Port, 21mm Straight Shaft, Female Connector on Irrigation Line and Male Connecter on Aspirating Line, 45mm Overall Length, Stainless Steel
- Database Sync Date
- 2026-08-09 09:03:52
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MR PHACO?
The registered manufacturer of record for MR PHACO is Crestpoint Management Limited.
What is the Primary UDI-DI identifier for MR PHACO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PH85112.
What classification code is assigned to this device?
This device is registered under product classification code HMX.
Similar Classification Devices (HMX)
Other Devices by Crestpoint Management Limited
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