gudid
Primary ID: PH9502T
MR PHACO (UDI PH9502T)
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 PH9502T
Device Regulatory Overview
The MR PHACO (Model/Catalog Number: PH9502T) is a medical device manufactured by Crestpoint Management Limited. This product is indexed under FDA Product Code / Category Classification HNH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PH9502T
- Product Code / EMDN
- HNH
- Device Name
- Globe Fixation Ring Fixed, 16mm OD x 12mm ID, FULL Style Head, Fine concentric grooves, Round Knurled Handle, 100mm Overall Length, Titanium
- 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 PH9502T.
What classification code is assigned to this device?
This device is registered under product classification code HNH.
Similar Classification Devices (HNH)
Other Devices by Crestpoint Management Limited
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