eudamed_udi
Primary ID: 08054329820018
LASER PER FISIOTERAPIA LASERIX PH3 (UDI 08054329820018)
Manufactured by GN MED s.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LASER PER FISIOTERAPIA LASERIX PH3 - Primary ID 08054329820018
Device Regulatory Overview
The LASER PER FISIOTERAPIA LASERIX PH3 (Model/Catalog Number: LASERIX PH3) is a medical device manufactured by GN MED s.r.l.. This product is indexed under FDA Product Code / Category Classification Z120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LASERIX PH3
- Product Code / EMDN
- Z120602
- Device Name
- LASER PER FISIOTERAPIA LASERIX PH3
- Database Sync Date
- 2026-08-09 16:29:09
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 LASER PER FISIOTERAPIA LASERIX PH3?
The registered manufacturer of record for LASER PER FISIOTERAPIA LASERIX PH3 is GN MED s.r.l..
What is the Primary UDI-DI identifier for LASER PER FISIOTERAPIA LASERIX PH3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054329820018.
What classification code is assigned to this device?
This device is registered under product classification code Z120602.
Similar Classification Devices (Z120602)
Other Devices by GN MED s.r.l.
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