gudid
Primary ID: PH9822
MR PHACO (UDI PH9822)
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 PH9822
Device Regulatory Overview
The MR PHACO (Model/Catalog Number: PH9822) is a medical device manufactured by Crestpoint Management Limited. This product is indexed under FDA Product Code / Category Classification HMR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PH9822
- Product Code / EMDN
- HMR
- Device Name
- Anis Radial Marker, 16 Radial Blades, 4.0mm Diameter Center Opening, Flat Handle, 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 PH9822.
What classification code is assigned to this device?
This device is registered under product classification code HMR.
Similar Classification Devices (HMR)
Other Devices by Crestpoint Management Limited
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