gudid
Primary ID: 410-230-170
RZ Medizintechnik GmbH (UDI 410-230-170)
Manufactured by RZ-Medizintechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RZ Medizintechnik GmbH - Primary ID 410-230-170
Device Regulatory Overview
The RZ Medizintechnik GmbH (Model/Catalog Number: 410-230-170) is a medical device manufactured by RZ-Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification KAK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 410-230-170
- Product Code / EMDN
- KAK
- Device Name
- HOUSE OVAL Window Pick, 30 angled 170mm, Octagon handle, pointed, 0.33mm malleable
- Database Sync Date
- 2026-08-09 09:11:24
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 RZ Medizintechnik GmbH?
The registered manufacturer of record for RZ Medizintechnik GmbH is RZ-Medizintechnik GmbH.
What is the Primary UDI-DI identifier for RZ Medizintechnik GmbH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 410-230-170.
What classification code is assigned to this device?
This device is registered under product classification code KAK.
Similar Classification Devices (KAK)
Other Devices by RZ-Medizintechnik GmbH
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