gudid
Primary ID: 8121-2
Power Dental USA (UDI 8121-2)
Manufactured by Power Dental U.S.A. Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Power Dental USA - Primary ID 8121-2
Device Regulatory Overview
The Power Dental USA (Model/Catalog Number: 8121-2) is a medical device manufactured by Power Dental U.S.A. Inc.. This product is indexed under FDA Product Code / Category Classification MDM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8121-2
- Product Code / EMDN
- MDM
- Device Name
- PIEZO BONE SURGERY TIPS FOR SURGIMASTER AND SURGIMASTER II,DCA7 Crestal approach tip 7mm with internal irrigation
- Database Sync Date
- 2026-08-09 09:01:11
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 Power Dental USA?
The registered manufacturer of record for Power Dental USA is Power Dental U.S.A. Inc..
What is the Primary UDI-DI identifier for Power Dental USA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8121-2.
What classification code is assigned to this device?
This device is registered under product classification code MDM.
Similar Classification Devices (MDM)
Other Devices by Power Dental U.S.A. Inc.
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