SYNCHRO 14 (UDI M00313320)
Manufactured by Stryker Corporation
Device Regulatory Overview
The SYNCHRO 14 (Model/Catalog Number: M00313320) is a medical device manufactured by Stryker Corporation. This product is indexed under FDA Product Code / Category Classification DQX 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
- M00313320
- Product Code / EMDN
- DQX
- Device Name
- Neuro Guidewire with Hydrophilic Coating
- Database Sync Date
- 2026-08-09 09:00:28
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 SYNCHRO 14?
The registered manufacturer of record for SYNCHRO 14 is Stryker Corporation.
What is the Primary UDI-DI identifier for SYNCHRO 14?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M00313320.
What classification code is assigned to this device?
This device is registered under product classification code DQX.
Similar Classification Devices (DQX)
Other Devices by Stryker Corporation
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