eudamed_udi
Primary ID: 08809815658237
Trephine Drill (UDI 08809815658237)
Manufactured by Neobiotech Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Trephine Drill - Primary ID 08809815658237
Device Regulatory Overview
The Trephine Drill (Model/Catalog Number: TB39) 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
- TB39
- Product Code / EMDN
- P01020101
- Device Name
- TB39
- Database Sync Date
- 2026-08-09 16:29:44
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 Trephine Drill?
The registered manufacturer of record for Trephine Drill is Neobiotech Co.,Ltd..
What is the Primary UDI-DI identifier for Trephine Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809815658237.
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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