gudid
Primary ID: 1622
Power Dental USA (UDI 1622)
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 1622
Device Regulatory Overview
The Power Dental USA (Model/Catalog Number: 1622) is a medical device manufactured by Power Dental U.S.A. Inc.. This product is indexed under FDA Product Code / Category Classification EMK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1622
- Product Code / EMDN
- EMK
- Device Name
- CURETTES SUB GRACEY SUB13/14
- Database Sync Date
- 2026-08-09 09:01:13
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 1622.
What classification code is assigned to this device?
This device is registered under product classification code EMK.
Similar Classification Devices (EMK)
Other Devices by Power Dental U.S.A. Inc.
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