eudamed_udi
Primary ID: 07640161462021
B.Box Professional (UDI 07640161462021)
Manufactured by BEMER Int. AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for B.Box Professional - Primary ID 07640161462021
Device Regulatory Overview
The B.Box Professional (Model/Catalog Number: 420200) 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
- 420200
- Product Code / EMDN
- Z12062801
- Device Name
- B.Box Professional
- Database Sync Date
- 2026-08-09 19:07:37
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 B.Box Professional?
The registered manufacturer of record for B.Box Professional is BEMER Int. AG.
What is the Primary UDI-DI identifier for B.Box Professional?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640161462021.
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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