gudid
Primary ID: SU-9-0079-12
Halstead Forceps (UDI SU-9-0079-12)
Manufactured by ELMED INSTRUMENTS(PVT)LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Halstead Forceps - Primary ID SU-9-0079-12
Device Regulatory Overview
The Halstead Forceps (Model/Catalog Number: SU-9-0079-12) is a medical device manufactured by ELMED INSTRUMENTS(PVT)LTD.. This product is indexed under FDA Product Code / Category Classification HRQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SU-9-0079-12
- Product Code / EMDN
- HRQ
- Device Name
- Intended Use: used for clamping vessels and controlling blow flow and other clamping tasks in general surgical procedures.Packaging: 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
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Halstead Forceps?
The registered manufacturer of record for Halstead Forceps is ELMED INSTRUMENTS(PVT)LTD..
What is the Primary UDI-DI identifier for Halstead Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SU-9-0079-12.
What classification code is assigned to this device?
This device is registered under product classification code HRQ.
Similar Classification Devices (HRQ)
Other Devices by ELMED INSTRUMENTS(PVT)LTD.
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