gudid
Primary ID: 10402
Fluorilaq Salted Caramel (10mL) Tube (UDI 10402)
Manufactured by PASCAL COMPANY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fluorilaq Salted Caramel (10mL) Tube - Primary ID 10402
Device Regulatory Overview
The Fluorilaq Salted Caramel (10mL) Tube (Model/Catalog Number: 10402) is a medical device manufactured by PASCAL COMPANY, INC.. This product is indexed under FDA Product Code / Category Classification LBH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10402
- Product Code / EMDN
- LBH
- Device Name
- 5% Sodium Fluoride with Xylitol. No separation, no mixing & no mess. Ideal for hypersensitivity treatments.
- Database Sync Date
- 2026-08-09 09:20:12
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 Fluorilaq Salted Caramel (10mL) Tube?
The registered manufacturer of record for Fluorilaq Salted Caramel (10mL) Tube is PASCAL COMPANY, INC..
What is the Primary UDI-DI identifier for Fluorilaq Salted Caramel (10mL) Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10402.
What classification code is assigned to this device?
This device is registered under product classification code LBH.
Similar Classification Devices (LBH)
Other Devices by PASCAL COMPANY, INC.
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