gudid
Primary ID: ST321313
ELMED INCORPORATED (UDI ST321313)
Manufactured by ELMED INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELMED INCORPORATED - Primary ID ST321313
Device Regulatory Overview
The ELMED INCORPORATED (Model/Catalog Number: ST321313) 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
- ST321313
- Product Code / EMDN
- HDF
- Device Name
- SPECULUM SURGICAL VAGINAL PEDERSON LARGE BLADE 121 MM LENGTH 26 MM WIDTH NOT WEIGHTED OPEN LEFT SIDE ADULT
- Database Sync Date
- 2026-08-09 09:00:28
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 INCORPORATED?
The registered manufacturer of record for ELMED INCORPORATED is ELMED INCORPORATED.
What is the Primary UDI-DI identifier for ELMED INCORPORATED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ST321313.
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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