gudid
Primary ID: G35271
Hercules (UDI G35271)
Manufactured by COOK INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hercules - Primary ID G35271
Device Regulatory Overview
The Hercules (Model/Catalog Number: G35271) is a medical device manufactured by COOK INCORPORATED. This product is indexed under FDA Product Code / Category Classification KCF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G35271
- Product Code / EMDN
- KCF
- Device Name
- Hercules 100 Transnasal Esophageal Balloon
- Database Sync Date
- 2026-08-09 09:33:19
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 Hercules?
The registered manufacturer of record for Hercules is COOK INCORPORATED.
What is the Primary UDI-DI identifier for Hercules?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G35271.
What classification code is assigned to this device?
This device is registered under product classification code KCF.
Similar Classification Devices (KCF)
Other Devices by COOK INCORPORATED
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