eudamed_udi
Primary ID: 08809486290538
IT cemented abutment_SCRP (UDI 08809486290538)
Manufactured by Neobiotech Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IT cemented abutment_SCRP - Primary ID 08809486290538
Device Regulatory Overview
The IT cemented abutment_SCRP (Model/Catalog Number: ICSW710) 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
- ICSW710
- Product Code / EMDN
- P01020101
- Device Name
- ICSW710
- Database Sync Date
- 2026-08-09 16:28:53
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 IT cemented abutment_SCRP?
The registered manufacturer of record for IT cemented abutment_SCRP is Neobiotech Co.,Ltd..
What is the Primary UDI-DI identifier for IT cemented abutment_SCRP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809486290538.
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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