eudamed_udi
Primary ID: 08800263100668
IS Hex Pick-up Impression Coping (UDI 08800263100668)
Manufactured by Neobiotech Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IS Hex Pick-up Impression Coping - Primary ID 08800263100668
Device Regulatory Overview
The IS Hex Pick-up Impression Coping (Model/Catalog Number: ISIPHL711P) is a medical device manufactured by Neobiotech Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification P01020180 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ISIPHL711P
- Product Code / EMDN
- P01020180
- Device Name
- Dental Surgical Instrument
- Database Sync Date
- 2026-08-09 16:28:54
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 IS Hex Pick-up Impression Coping?
The registered manufacturer of record for IS Hex Pick-up Impression Coping is Neobiotech Co.,Ltd..
What is the Primary UDI-DI identifier for IS Hex Pick-up Impression Coping?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800263100668.
What classification code is assigned to this device?
This device is registered under product classification code P01020180.
Similar Classification Devices (P01020180)
Other Devices by Neobiotech Co.,Ltd.
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