Synchron (UDI 475009)
Manufactured by Beckman Coulter, Inc.
Device Regulatory Overview
The Synchron (Model/Catalog Number: 475009) is a medical device manufactured by Beckman Coulter, Inc.. This product is indexed under FDA Product Code / Category Classification LCM within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 475009
- Product Code / EMDN
- LCM
- Device Name
- Phencyclidine Reagent (PCP 1 x 250)
- Database Sync Date
- 2026-08-09 09:22:51
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 Synchron?
The registered manufacturer of record for Synchron is Beckman Coulter, Inc..
What is the Primary UDI-DI identifier for Synchron?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 475009.
What classification code is assigned to this device?
This device is registered under product classification code LCM.
Similar Classification Devices (LCM)
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