gudid
Primary ID: MSK111605
ESI (UDI MSK111605)
Manufactured by FTT MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ESI - Primary ID MSK111605
Device Regulatory Overview
The ESI (Model/Catalog Number: MSK111605) is a medical device manufactured by FTT MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification HJM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MSK111605
- Product Code / EMDN
- HJM
- Device Name
- MIRA TRANSILLUMINATOR/ PILLING EYE LIGHT. ACMI FITTING.
- Database Sync Date
- 2026-08-09 09:34:57
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 ESI?
The registered manufacturer of record for ESI is FTT MEDICAL, INC..
What is the Primary UDI-DI identifier for ESI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MSK111605.
What classification code is assigned to this device?
This device is registered under product classification code HJM.
Similar Classification Devices (HJM)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint