gudid
Primary ID: 12881-32-000
Valve (UDI 12881-32-000)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Valve - Primary ID 12881-32-000
Device Regulatory Overview
The Valve (Model/Catalog Number: 12881-32-000) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification FFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12881-32-000
- Product Code / EMDN
- FFO
- Device Name
- Valve Retractor for Oval Frame 12881-22
- Database Sync Date
- 2026-08-09 09:07:00
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 Valve?
The registered manufacturer of record for Valve is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for Valve?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12881-32-000.
What classification code is assigned to this device?
This device is registered under product classification code FFO.
Similar Classification Devices (FFO)
Other Devices by SONTEC INSTRUMENTS, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint