INFUSION CUFF 5000 ml with manometer, bladder and air release valve (UDI 04260157892385)
Manufactured by Friedrich Bosch GmbH&Co.KG
Device Regulatory Overview
The INFUSION CUFF 5000 ml with manometer, bladder and air release valve (Model/Catalog Number: 5001.11.030) is a medical device manufactured by Friedrich Bosch GmbH&Co.KG. This product is indexed under FDA Product Code / Category Classification Z12030399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5001.11.030
- Product Code / EMDN
- Z12030399
- Device Name
- INFUSION CUFF
- Database Sync Date
- 2026-08-09 17:21:59
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 INFUSION CUFF 5000 ml with manometer, bladder and air release valve?
The registered manufacturer of record for INFUSION CUFF 5000 ml with manometer, bladder and air release valve is Friedrich Bosch GmbH&Co.KG.
What is the Primary UDI-DI identifier for INFUSION CUFF 5000 ml with manometer, bladder and air release valve?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260157892385.
What classification code is assigned to this device?
This device is registered under product classification code Z12030399.
Similar Classification Devices (Z12030399)
Other Devices by Friedrich Bosch GmbH&Co.KG
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