Presbyterian Tube Occluding Forceps (UDI SU-9-0721-18)
Manufactured by ELMED INSTRUMENTS(PVT)LTD.
Device Regulatory Overview
The Presbyterian Tube Occluding Forceps (Model/Catalog Number: SU-9-0721-18) is a medical device manufactured by ELMED INSTRUMENTS(PVT)LTD.. This product is indexed under FDA Product Code / Category Classification GDJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SU-9-0721-18
- Product Code / EMDN
- GDJ
- Device Name
- Intended Use: used to control the flow of fluidsPackaging: Packaging shall be as per customer requirements e.g set of 25 or set of 50.
- Database Sync Date
- 2026-08-09 09:04:00
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 Presbyterian Tube Occluding Forceps?
The registered manufacturer of record for Presbyterian Tube Occluding Forceps is ELMED INSTRUMENTS(PVT)LTD..
What is the Primary UDI-DI identifier for Presbyterian Tube Occluding Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SU-9-0721-18.
What classification code is assigned to this device?
This device is registered under product classification code GDJ.
Similar Classification Devices (GDJ)
Other Devices by ELMED INSTRUMENTS(PVT)LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint