gudid
Primary ID: 05-0112
ESI (UDI 05-0112)
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 05-0112
Device Regulatory Overview
The ESI (Model/Catalog Number: 05-0112) 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
- 05-0112
- Product Code / EMDN
- HJM
- Device Name
- 1/8" DIAMETER TRANSILLUMINATOR, ACMI FITTING.
- Database Sync Date
- 2026-08-09 09:34:57
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 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 05-0112.
What classification code is assigned to this device?
This device is registered under product classification code HJM.
Similar Classification Devices (HJM)
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