eudamed_udi
Primary ID: 00606959021600
Patient Circuit, CA Infant (UDI 00606959021600)
Manufactured by Respironics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Patient Circuit, CA Infant - Primary ID 00606959021600
Device Regulatory Overview
The Patient Circuit, CA Infant (Model/Catalog Number: 325-9237) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 325-9237
- Product Code / EMDN
- R05010301
- Device Name
- Patient Circuit, CA Infant
- Database Sync Date
- 2026-08-09 17:06:40
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 Patient Circuit, CA Infant?
The registered manufacturer of record for Patient Circuit, CA Infant is Respironics Inc..
What is the Primary UDI-DI identifier for Patient Circuit, CA Infant?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959021600.
What classification code is assigned to this device?
This device is registered under product classification code R05010301.
Similar Classification Devices (R05010301)
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