gudid
Primary ID: CM-3201-102
Huestis Medical Collimator (UDI CM-3201-102)
Manufactured by HUESTIS MACHINE CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Huestis Medical Collimator - Primary ID CM-3201-102
Device Regulatory Overview
The Huestis Medical Collimator (Model/Catalog Number: CM-3201-102) is a medical device manufactured by HUESTIS MACHINE CORPORATION. This product is indexed under FDA Product Code / Category Classification IZX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CM-3201-102
- Product Code / EMDN
- IZX
- Device Name
- 150PBL/SC Collimator (Huestis Part # CM-3201-102)
- Database Sync Date
- 2026-08-09 09:37:37
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 Huestis Medical Collimator?
The registered manufacturer of record for Huestis Medical Collimator is HUESTIS MACHINE CORPORATION.
What is the Primary UDI-DI identifier for Huestis Medical Collimator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CM-3201-102.
What classification code is assigned to this device?
This device is registered under product classification code IZX.
Similar Classification Devices (IZX)
Other Devices by HUESTIS MACHINE CORPORATION
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