eudamed_udi
Primary ID: +EINV300531001B
Cystoscope (UDI +EINV300531001B)
Manufactured by Innoview GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cystoscope - Primary ID +EINV300531001B
Device Regulatory Overview
The Cystoscope (Model/Catalog Number: 30-0531-00) is a medical device manufactured by Innoview GmbH. This product is indexed under FDA Product Code / Category Classification Z12020701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30-0531-00
- Product Code / EMDN
- Z12020701
- Device Name
- Rigid Endoscope
- Database Sync Date
- 2026-08-09 16:47:14
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 Cystoscope?
The registered manufacturer of record for Cystoscope is Innoview GmbH.
What is the Primary UDI-DI identifier for Cystoscope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +EINV300531001B.
What classification code is assigned to this device?
This device is registered under product classification code Z12020701.
Similar Classification Devices (Z12020701)
Other Devices by Innoview GmbH
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