gudid
Primary ID: 0011507FG
Sodium Hypochlorite Solution (UDI 0011507FG)
Manufactured by DENTSPLY INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sodium Hypochlorite Solution - Primary ID 0011507FG
Device Regulatory Overview
The Sodium Hypochlorite Solution (Model/Catalog Number: 0011507FG) is a medical device manufactured by DENTSPLY INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification KJJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0011507FG
- Product Code / EMDN
- KJJ
- Device Name
- Sodium Hypochlorite Solution 16 oz.
- Database Sync Date
- 2026-08-09 09:03:03
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 Sodium Hypochlorite Solution?
The registered manufacturer of record for Sodium Hypochlorite Solution is DENTSPLY INTERNATIONAL INC..
What is the Primary UDI-DI identifier for Sodium Hypochlorite Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0011507FG.
What classification code is assigned to this device?
This device is registered under product classification code KJJ.
Similar Classification Devices (KJJ)
Other Devices by DENTSPLY INTERNATIONAL INC.
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