gudid
Primary ID: WF100
Wire Fixation (UDI WF100)
Manufactured by BIOACCESS INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wire Fixation - Primary ID WF100
Device Regulatory Overview
The Wire Fixation (Model/Catalog Number: WF100) is a medical device manufactured by BIOACCESS INC. This product is indexed under FDA Product Code / Category Classification GFF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WF100
- Product Code / EMDN
- GFF
- Device Name
- Database Sync Date
- 2026-08-09 09:45:02
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Wire Fixation?
The registered manufacturer of record for Wire Fixation is BIOACCESS INC.
What is the Primary UDI-DI identifier for Wire Fixation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WF100.
What classification code is assigned to this device?
This device is registered under product classification code GFF.
Similar Classification Devices (GFF)
Other Devices by BIOACCESS INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint