gudid
Primary ID: MSK082714
ESI (UDI MSK082714)
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 MSK082714
Device Regulatory Overview
The ESI (Model/Catalog Number: MSK082714) is a medical device manufactured by FTT MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification GCF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MSK082714
- Product Code / EMDN
- GCF
- Device Name
- CUSTOM YEOMAN LIGHT CARRIER FOR CODMAN RETRACTOR.
- 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 MSK082714.
What classification code is assigned to this device?
This device is registered under product classification code GCF.
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