eudamed_udi
Primary ID: 08050714660672
RECLINE REV (UDI 08050714660672)
Manufactured by Technogym spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RECLINE REV - Primary ID 08050714660672
Device Regulatory Overview
The RECLINE REV (Model/Catalog Number: DFDM3A0) is a medical device manufactured by Technogym spa. This product is indexed under FDA Product Code / Category Classification Z120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DFDM3A0
- Product Code / EMDN
- Z120602
- Device Name
- RECLINE REV
- Database Sync Date
- 2026-08-09 16:29:20
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 RECLINE REV?
The registered manufacturer of record for RECLINE REV is Technogym spa.
What is the Primary UDI-DI identifier for RECLINE REV?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050714660672.
What classification code is assigned to this device?
This device is registered under product classification code Z120602.
Similar Classification Devices (Z120602)
Other Devices by Technogym spa
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