gudid
Primary ID: SBC-460
Seal (UDI SBC-460)
Manufactured by ENDOCHOICE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Seal - Primary ID SBC-460
Device Regulatory Overview
The Seal (Model/Catalog Number: SBC-460) is a medical device manufactured by ENDOCHOICE, INC.. This product is indexed under FDA Product Code / Category Classification OCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SBC-460
- Product Code / EMDN
- OCX
- Device Name
- Biopsy Valve
- Database Sync Date
- 2026-08-09 09:12:11
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 Seal?
The registered manufacturer of record for Seal is ENDOCHOICE, INC..
What is the Primary UDI-DI identifier for Seal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SBC-460.
What classification code is assigned to this device?
This device is registered under product classification code OCX.
Similar Classification Devices (OCX)
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