gudid
Primary ID: 290-850-240
RZ Medizintechnik GmbH (UDI 290-850-240)
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 290-850-240
Device Regulatory Overview
The RZ Medizintechnik GmbH (Model/Catalog Number: 290-850-240) is a medical device manufactured by RZ-Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification GEN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 290-850-240
- Product Code / EMDN
- GEN
- Device Name
- DeBakey Monopolar Atraumatic Forceps straight, 1,5mm tip, insulated, 240mm 9 1/2"
- Database Sync Date
- 2026-08-09 09:11:23
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 290-850-240.
What classification code is assigned to this device?
This device is registered under product classification code GEN.
Similar Classification Devices (GEN)
Other Devices by RZ-Medizintechnik GmbH
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