gudid
Primary ID: 6070540127
ADULT FLOSSER PIKS (UDI 6070540127)
Manufactured by MAXILL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ADULT FLOSSER PIKS - Primary ID 6070540127
Device Regulatory Overview
The ADULT FLOSSER PIKS (Model/Catalog Number: 6070540127) is a medical device manufactured by MAXILL, INC.. This product is indexed under FDA Product Code / Category Classification JES within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6070540127
- Product Code / EMDN
- JES
- Device Name
- Database Sync Date
- 2026-08-09 09:03:34
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 ADULT FLOSSER PIKS?
The registered manufacturer of record for ADULT FLOSSER PIKS is MAXILL, INC..
What is the Primary UDI-DI identifier for ADULT FLOSSER PIKS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6070540127.
What classification code is assigned to this device?
This device is registered under product classification code JES.
Similar Classification Devices (JES)
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