gudid
Primary ID: PH9517T
MR PHACO (UDI PH9517T)
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 PH9517T
Device Regulatory Overview
The MR PHACO (Model/Catalog Number: PH9517T) 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
- PH9517T
- Product Code / EMDN
- HMR
- Device Name
- Toric IOL Reference Marker Blades are positioned at 0, 90, 180 Degrees, Head is angled at 70 degrees, Round Knurled Handle, 98mm Overall Length, Titanium
- Database Sync Date
- 2026-08-09 09:03:52
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 PH9517T.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint