gudid
Primary ID: BFX110
Paul Banditt (UDI BFX110)
Manufactured by Terlain Enterprises, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Paul Banditt - Primary ID BFX110
Device Regulatory Overview
The Paul Banditt (Model/Catalog Number: BFX110) is a medical device manufactured by Terlain Enterprises, Inc.. This product is indexed under FDA Product Code / Category Classification EMI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BFX110
- Product Code / EMDN
- EMI
- Device Name
- PAUL BANDITT 110 BONE FILE, CROSS CUT, OCTAGONAL HANDLE, DE
- Database Sync Date
- 2026-08-09 09:01:11
Full Regulatory Attributes
🔒 Token Gated
{
"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 Paul Banditt?
The registered manufacturer of record for Paul Banditt is Terlain Enterprises, Inc..
What is the Primary UDI-DI identifier for Paul Banditt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BFX110.
What classification code is assigned to this device?
This device is registered under product classification code EMI.
Similar Classification Devices (EMI)
Other Devices by Terlain Enterprises, Inc.
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