gudid
Primary ID: 801 007
N/A (UDI 801 007)
Manufactured by inomed Medizintechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 801 007
Device Regulatory Overview
The N/A (Model/Catalog Number: 801 007) is a medical device manufactured by inomed Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification DZP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 801 007
- Product Code / EMDN
- DZP
- Device Name
- RM Vertical Arc 85
- Database Sync Date
- 2026-08-09 09:07:45
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 inomed Medizintechnik GmbH.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 801 007.
What classification code is assigned to this device?
This device is registered under product classification code DZP.
Similar Classification Devices (DZP)
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