eudamed_udi
Primary ID: 04260157893467
Manometer Claude (UDI 04260157893467)
Manufactured by Friedrich Bosch GmbH&Co.KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Manometer Claude - Primary ID 04260157893467
Device Regulatory Overview
The Manometer Claude (Model/Catalog Number: 9019.00.001) is a medical device manufactured by Friedrich Bosch GmbH&Co.KG. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9019.00.001
- Product Code / EMDN
- C9006
- Device Name
- Sphygmomanometers
- Database Sync Date
- 2026-08-09 16:48:30
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 Manometer Claude?
The registered manufacturer of record for Manometer Claude is Friedrich Bosch GmbH&Co.KG.
What is the Primary UDI-DI identifier for Manometer Claude?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260157893467.
What classification code is assigned to this device?
This device is registered under product classification code C9006.
Similar Classification Devices (C9006)
Other Devices by Friedrich Bosch GmbH&Co.KG
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