Dpex I (UDI 06944843603056)
Manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.
Device Regulatory Overview
The Dpex I (Model/Catalog Number: Z1211) is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12110101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Z1211
- Product Code / EMDN
- Z12110101
- Device Name
- Apex Locator
- Database Sync Date
- 2026-08-09 16:28:44
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 Dpex I?
The registered manufacturer of record for Dpex I is Guilin Woodpecker Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for Dpex I?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944843603056.
What classification code is assigned to this device?
This device is registered under product classification code Z12110101.
Similar Classification Devices (Z12110101)
Other Devices by Guilin Woodpecker Medical Instrument Co., Ltd.
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