eudamed_udi
Primary ID: 03770011904174
Recharge AP214 douce (UDI 03770011904174)
Manufactured by JLB FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Recharge AP214 douce - Primary ID 03770011904174
Device Regulatory Overview
The Recharge AP214 douce (Model/Catalog Number: AP214FS) is a medical device manufactured by JLB FRANCE. This product is indexed under FDA Product Code / Category Classification Z12069080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AP214FS
- Product Code / EMDN
- Z12069080
- Device Name
- G5 Massage Applicators
- Database Sync Date
- 2026-08-09 19:01:59
Full Regulatory Attributes
đź”’ 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 Recharge AP214 douce?
The registered manufacturer of record for Recharge AP214 douce is JLB FRANCE.
What is the Primary UDI-DI identifier for Recharge AP214 douce?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770011904174.
What classification code is assigned to this device?
This device is registered under product classification code Z12069080.
Similar Classification Devices (Z12069080)
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