eudamed_udi
Primary ID: 07640161460690
Light Pack Evo (UDI 07640161460690)
Manufactured by BEMER Int. AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Light Pack Evo - Primary ID 07640161460690
Device Regulatory Overview
The Light Pack Evo (Model/Catalog Number: 415000) is a medical device manufactured by BEMER Int. AG. This product is indexed under FDA Product Code / Category Classification Z12040202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 415000
- Product Code / EMDN
- Z12040202
- Device Name
- BEMER Therapy System Evo
- Database Sync Date
- 2026-08-09 18:03:30
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 Light Pack Evo?
The registered manufacturer of record for Light Pack Evo is BEMER Int. AG.
What is the Primary UDI-DI identifier for Light Pack Evo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640161460690.
What classification code is assigned to this device?
This device is registered under product classification code Z12040202.
Similar Classification Devices (Z12040202)
Other Devices by BEMER Int. AG
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