Scoopboard (UDI 04260178352899)
Manufactured by GS Elektromedizinische Geräte G. Stemple GmbH
Device Regulatory Overview
The Scoopboard (Model/Catalog Number: 09302) is a medical device manufactured by GS Elektromedizinische Geräte G. Stemple GmbH. This product is indexed under FDA Product Code / Category Classification Z120304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 09302
- Product Code / EMDN
- Z120304
- Device Name
- boards
- Database Sync Date
- 2026-08-09 16:28:54
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 Scoopboard?
The registered manufacturer of record for Scoopboard is GS Elektromedizinische Geräte G. Stemple GmbH.
What is the Primary UDI-DI identifier for Scoopboard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260178352899.
What classification code is assigned to this device?
This device is registered under product classification code Z120304.
Similar Classification Devices (Z120304)
Other Devices by GS Elektromedizinische Geräte G. Stemple GmbH
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