woodpecker (UDI Endo Space)
Manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.
Device Regulatory Overview
The woodpecker (Model/Catalog Number: Endo Space) is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification EKX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Endo Space
- Product Code / EMDN
- EKX
- Device Name
- endo motor
- 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 woodpecker?
The registered manufacturer of record for woodpecker is Guilin Woodpecker Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for woodpecker?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Endo Space.
What classification code is assigned to this device?
This device is registered under product classification code EKX.
Similar Classification Devices (EKX)
Other Devices by Guilin Woodpecker Medical Instrument Co., Ltd.
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