gudid
Primary ID: ST321011A
ELMED (UDI ST321011A)
Manufactured by ELMED INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELMED - Primary ID ST321011A
Device Regulatory Overview
The ELMED (Model/Catalog Number: ST321011A) is a medical device manufactured by ELMED INCORPORATED. This product is indexed under FDA Product Code / Category Classification HDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ST321011A
- Product Code / EMDN
- HDF
- Device Name
- WEISMAN GRAVES VAGINAL SPECULUM- RIGHT SIDE OPEN 45 deg HANDLE, SMALL, 3" X 1"
- Database Sync Date
- 2026-08-09 09:13:31
Full Regulatory Attributes
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{
"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 ELMED?
The registered manufacturer of record for ELMED is ELMED INCORPORATED.
What is the Primary UDI-DI identifier for ELMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ST321011A.
What classification code is assigned to this device?
This device is registered under product classification code HDF.
Similar Classification Devices (HDF)
Other Devices by ELMED INCORPORATED
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