gudid
Primary ID: 80085003
n/a (UDI 80085003)
Manufactured by implantcast GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for n/a - Primary ID 80085003
Device Regulatory Overview
The n/a (Model/Catalog Number: 80085003) is a medical device manufactured by implantcast GmbH. This product is indexed under FDA Product Code / Category Classification HTO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80085003
- Product Code / EMDN
- HTO
- Device Name
- calcar reamer Hudson
- Database Sync Date
- 2026-08-09 09:11:29
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 n/a?
The registered manufacturer of record for n/a is implantcast GmbH.
What is the Primary UDI-DI identifier for n/a?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80085003.
What classification code is assigned to this device?
This device is registered under product classification code HTO.
Similar Classification Devices (HTO)
Other Devices by implantcast GmbH
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