ENDORAL ELECTRIC MASSAGE EQUIPMENT (UDI Z120612)
Device Regulatory Overview
The ENDORAL ELECTRIC MASSAGE EQUIPMENT (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification Z120612 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Z120612
- Device Name
- ENDORAL ELECTRIC MASSAGE EQUIPMENT
- Database Sync Date
- 2026-08-09 16:18:37
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 ENDORAL ELECTRIC MASSAGE EQUIPMENT?
The registered manufacturer of record for ENDORAL ELECTRIC MASSAGE EQUIPMENT is .
What is the Primary UDI-DI identifier for ENDORAL ELECTRIC MASSAGE EQUIPMENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z120612.
What classification code is assigned to this device?
This device is registered under product classification code Z120612.
Similar Classification Devices (Z120612)
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