eudamed_udi
Primary ID: +EINV300039001E
Rhinoscope/ Sinuscope (UDI +EINV300039001E)
Manufactured by Innoview GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rhinoscope/ Sinuscope - Primary ID +EINV300039001E
Device Regulatory Overview
The Rhinoscope/ Sinuscope (Model/Catalog Number: 30-0039-00) is a medical device manufactured by Innoview GmbH. This product is indexed under FDA Product Code / Category Classification Z12021008 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30-0039-00
- Product Code / EMDN
- Z12021008
- Device Name
- Rigid Endoscope
- Database Sync Date
- 2026-08-09 16:29:00
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 Rhinoscope/ Sinuscope?
The registered manufacturer of record for Rhinoscope/ Sinuscope is Innoview GmbH.
What is the Primary UDI-DI identifier for Rhinoscope/ Sinuscope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +EINV300039001E.
What classification code is assigned to this device?
This device is registered under product classification code Z12021008.
Similar Classification Devices (Z12021008)
Other Devices by Innoview GmbH
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