eudamed_udi
Primary ID: 04034393711164
IVOM-OP-Set (UDI 04034393711164)
Manufactured by Sengewald Klinikprodukte GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IVOM-OP-Set - Primary ID 04034393711164
Device Regulatory Overview
The IVOM-OP-Set (Model/Catalog Number: 66226474-01) is a medical device manufactured by Sengewald Klinikprodukte GmbH. This product is indexed under FDA Product Code / Category Classification A010599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 66226474-01
- Product Code / EMDN
- A010599
- Device Name
- IVOM-Set
- Database Sync Date
- 2026-08-09 16:28:51
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 IVOM-OP-Set?
The registered manufacturer of record for IVOM-OP-Set is Sengewald Klinikprodukte GmbH.
What is the Primary UDI-DI identifier for IVOM-OP-Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04034393711164.
What classification code is assigned to this device?
This device is registered under product classification code A010599.
Similar Classification Devices (A010599)
Other Devices by Sengewald Klinikprodukte GmbH
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