gudid
Primary ID: T70203
MR PHACO (UDI T70203)
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 T70203
Device Regulatory Overview
The MR PHACO (Model/Catalog Number: T70203) is a medical device manufactured by Crestpoint Management Limited. This product is indexed under FDA Product Code / Category Classification FSM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T70203
- Product Code / EMDN
- FSM
- Device Name
- Microsurgical Plastic Instrument Sterilization Tray, 10"W x 15" L x 1.5" H deep base, lid, and silicone finger mat, accommodates 25-35 instruments
- 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 T70203.
What classification code is assigned to this device?
This device is registered under product classification code FSM.
Similar Classification Devices (FSM)
Other Devices by Crestpoint Management Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint