DTE (UDI Implanter)
Manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.
Device Regulatory Overview
The DTE (Model/Catalog Number: Implanter) is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification EBW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Implanter
- Product Code / EMDN
- EBW
- Device Name
- Mechanical drive unit with coolant supply for transmission instruments with ISO 3964 (DIN13940) compatible coupling system, for use in dental surgery, implantology andmaxillofacial surgery (CMF) for treatment of dental hard tissue.
- Database Sync Date
- 2026-08-09 09:11:05
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 DTE?
The registered manufacturer of record for DTE is Guilin Woodpecker Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for DTE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Implanter.
What classification code is assigned to this device?
This device is registered under product classification code EBW.
Similar Classification Devices (EBW)
Other Devices by Guilin Woodpecker Medical Instrument Co., Ltd.
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