gudid
Primary ID: 600B-F-400
MAXAPPLICATOR II (UDI 600B-F-400)
Manufactured by PLASDENT CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAXAPPLICATOR II - Primary ID 600B-F-400
Device Regulatory Overview
The MAXAPPLICATOR II (Model/Catalog Number: 600B-F-400) is a medical device manufactured by PLASDENT CORPORATION. This product is indexed under FDA Product Code / Category Classification KXF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 600B-F-400
- Product Code / EMDN
- KXF
- Device Name
- Applicators - Fine, Assorted 2 colors
- Database Sync Date
- 2026-08-09 09:03:38
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MAXAPPLICATOR II?
The registered manufacturer of record for MAXAPPLICATOR II is PLASDENT CORPORATION.
What is the Primary UDI-DI identifier for MAXAPPLICATOR II?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 600B-F-400.
What classification code is assigned to this device?
This device is registered under product classification code KXF.
Similar Classification Devices (KXF)
Other Devices by PLASDENT CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint