gudid
Primary ID: DSSH-1
Dentronix (UDI DSSH-1)
Manufactured by DENTRONIX INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dentronix - Primary ID DSSH-1
Device Regulatory Overview
The Dentronix (Model/Catalog Number: DSSH-1) is a medical device manufactured by DENTRONIX INC. This product is indexed under FDA Product Code / Category Classification KMH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DSSH-1
- Product Code / EMDN
- KMH
- Device Name
- Spore Strip Holder
- Database Sync Date
- 2026-08-09 09:03:07
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 Dentronix?
The registered manufacturer of record for Dentronix is DENTRONIX INC.
What is the Primary UDI-DI identifier for Dentronix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DSSH-1.
What classification code is assigned to this device?
This device is registered under product classification code KMH.
Similar Classification Devices (KMH)
Other Devices by DENTRONIX INC
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