Fergusson's suction cannula, d= 3 mm, 130 mm (UDI 05996660070628)
Manufactured by SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság
Device Regulatory Overview
The Fergusson's suction cannula, d= 3 mm, 130 mm (Model/Catalog Number: WD-441-30) is a medical device manufactured by SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság. This product is indexed under FDA Product Code / Category Classification L030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WD-441-30
- Product Code / EMDN
- L030199
- Device Name
- Probes, suction tubes, tampon holders, dilators
- Database Sync Date
- 2026-08-09 16:47:05
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 Fergusson's suction cannula, d= 3 mm, 130 mm?
The registered manufacturer of record for Fergusson's suction cannula, d= 3 mm, 130 mm is SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság.
What is the Primary UDI-DI identifier for Fergusson's suction cannula, d= 3 mm, 130 mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05996660070628.
What classification code is assigned to this device?
This device is registered under product classification code L030199.
Similar Classification Devices (L030199)
Other Devices by SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint