eudamed_udi
Primary ID: 07640161461024
BEMER Pro-Set (UDI 07640161461024)
Manufactured by BEMER Int. AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BEMER Pro-Set - Primary ID 07640161461024
Device Regulatory Overview
The BEMER Pro-Set (Model/Catalog Number: 410200) is a medical device manufactured by BEMER Int. AG. This product is indexed under FDA Product Code / Category Classification Z12062801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 410200
- Product Code / EMDN
- Z12062801
- Device Name
- BEMER Pro-Set
- Database Sync Date
- 2026-08-09 17:29:06
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 BEMER Pro-Set?
The registered manufacturer of record for BEMER Pro-Set is BEMER Int. AG.
What is the Primary UDI-DI identifier for BEMER Pro-Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640161461024.
What classification code is assigned to this device?
This device is registered under product classification code Z12062801.
Similar Classification Devices (Z12062801)
Other Devices by BEMER Int. AG
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