eudamed_udi
Primary ID: 08809815656165
NeoGuide Taper Drill (UDI 08809815656165)
Manufactured by Neobiotech Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoGuide Taper Drill - Primary ID 08809815656165
Device Regulatory Overview
The NeoGuide Taper Drill (Model/Catalog Number: NGTD4513) is a medical device manufactured by Neobiotech Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NGTD4513
- Product Code / EMDN
- P01020101
- Device Name
- NGTD4513
- Database Sync Date
- 2026-08-09 16:30:06
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 NeoGuide Taper Drill?
The registered manufacturer of record for NeoGuide Taper Drill is Neobiotech Co.,Ltd..
What is the Primary UDI-DI identifier for NeoGuide Taper Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809815656165.
What classification code is assigned to this device?
This device is registered under product classification code P01020101.
Similar Classification Devices (P01020101)
Other Devices by Neobiotech Co.,Ltd.
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