gudid
Primary ID: 66077539
Pala (UDI 66077539)
Manufactured by Kulzer GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pala - Primary ID 66077539
Device Regulatory Overview
The Pala (Model/Catalog Number: 66077539) is a medical device manufactured by Kulzer GmbH. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 66077539
- Product Code / EMDN
- EFT
- Device Name
- Pala Brillance Denture Cleanser 64 tab
- Database Sync Date
- 2026-08-09 09:09:38
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 Pala?
The registered manufacturer of record for Pala is Kulzer GmbH.
What is the Primary UDI-DI identifier for Pala?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66077539.
What classification code is assigned to this device?
This device is registered under product classification code EFT.
Similar Classification Devices (EFT)
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