eudamed_udi
Primary ID: 03700757609002
Rejulift (UDI 03700757609002)
Manufactured by S.A.R.L. MONTE-CARLO ESTHETICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rejulift - Primary ID 03700757609002
Device Regulatory Overview
The Rejulift (Model/Catalog Number: RJL) is a medical device manufactured by S.A.R.L. MONTE-CARLO ESTHETICS. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RJL
- Product Code / EMDN
- Z12069099
- Device Name
- Revitex
- Database Sync Date
- 2026-08-09 16:29:24
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 Rejulift?
The registered manufacturer of record for Rejulift is S.A.R.L. MONTE-CARLO ESTHETICS.
What is the Primary UDI-DI identifier for Rejulift?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700757609002.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by S.A.R.L. MONTE-CARLO ESTHETICS
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