Zantomed selectiv Dental-Einmal-Applikatoren regular blau (UDI 04260044630533)
Manufactured by Zantomed GmbH
Device Regulatory Overview
The Zantomed selectiv Dental-Einmal-Applikatoren regular blau (Model/Catalog Number: PP 901) is a medical device manufactured by Zantomed GmbH. This product is indexed under FDA Product Code / Category Classification Q019006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PP 901
- Product Code / EMDN
- Q019006
- Device Name
- Mikro-Applikatoren
- Database Sync Date
- 2026-08-09 16:29:38
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 Zantomed selectiv Dental-Einmal-Applikatoren regular blau?
The registered manufacturer of record for Zantomed selectiv Dental-Einmal-Applikatoren regular blau is Zantomed GmbH.
What is the Primary UDI-DI identifier for Zantomed selectiv Dental-Einmal-Applikatoren regular blau?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260044630533.
What classification code is assigned to this device?
This device is registered under product classification code Q019006.
Similar Classification Devices (Q019006)
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