GUDIDData
gudid Primary ID: T70021

MR PHACO (UDI T70021)

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 T70021

Device Regulatory Overview

The MR PHACO (Model/Catalog Number: T70021) 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
T70021
Product Code / EMDN
FSM
Device Name
Mini Plastic Instrument Sterilization Tray, 1.5"W x 2.75" L x 1.25" H deep base lid and silicone finger mat
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 T70021.

What classification code is assigned to this device?

This device is registered under product classification code FSM.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint