gudid
Primary ID: 2200-490
Bengolea Hemostatic Forceps (UDI 2200-490)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bengolea Hemostatic Forceps - Primary ID 2200-490
Device Regulatory Overview
The Bengolea Hemostatic Forceps (Model/Catalog Number: 2200-490) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HRQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2200-490
- Product Code / EMDN
- HRQ
- Device Name
- Bengolea Hemostatic Forceps Cross-Serrated Straight
- 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 Bengolea Hemostatic Forceps?
The registered manufacturer of record for Bengolea Hemostatic Forceps is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for Bengolea Hemostatic Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2200-490.
What classification code is assigned to this device?
This device is registered under product classification code HRQ.
Similar Classification Devices (HRQ)
Other Devices by SONTEC INSTRUMENTS, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint