Restrictor Capillary (UDI 55018)
Manufactured by Chromsystems Instruments + Chemicals GmbH
Device Regulatory Overview
The Restrictor Capillary (Model/Catalog Number: 55018) is a medical device manufactured by Chromsystems Instruments + Chemicals GmbH. This product is indexed under FDA Product Code / Category Classification KZR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 55018
- Product Code / EMDN
- KZR
- Device Name
- Restrictor Capillary
- Database Sync Date
- 2026-08-09 09:11:40
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 Restrictor Capillary?
The registered manufacturer of record for Restrictor Capillary is Chromsystems Instruments + Chemicals GmbH.
What is the Primary UDI-DI identifier for Restrictor Capillary?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 55018.
What classification code is assigned to this device?
This device is registered under product classification code KZR.
Similar Classification Devices (KZR)
Other Devices by Chromsystems Instruments + Chemicals GmbH
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