gudid
Primary ID: VIO-4
NA (UDI VIO-4)
Manufactured by Anspach Effort, The
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID VIO-4
Device Regulatory Overview
The NA (Model/Catalog Number: VIO-4) is a medical device manufactured by Anspach Effort, The. This product is indexed under FDA Product Code / Category Classification GFF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VIO-4
- Product Code / EMDN
- GFF
- Device Name
- 4 mm Fluted Ball. Use with B-VIOLET Attachment.
- Database Sync Date
- 2026-08-09 09:21:09
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 NA?
The registered manufacturer of record for NA is Anspach Effort, The.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VIO-4.
What classification code is assigned to this device?
This device is registered under product classification code GFF.
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