gudid
Primary ID: PH-320-210
PHASOR (UDI PH-320-210)
Manufactured by PHASOR HEALTH LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PHASOR - Primary ID PH-320-210
Device Regulatory Overview
The PHASOR (Model/Catalog Number: PH-320-210) is a medical device manufactured by PHASOR HEALTH LLC. This product is indexed under FDA Product Code / Category Classification HBE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PH-320-210
- Product Code / EMDN
- HBE
- Device Name
- Phasor Drill 3.20-mm diameter, length ~210-mm
- Database Sync Date
- 2026-08-09 09:06:29
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 PHASOR?
The registered manufacturer of record for PHASOR is PHASOR HEALTH LLC.
What is the Primary UDI-DI identifier for PHASOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PH-320-210.
What classification code is assigned to this device?
This device is registered under product classification code HBE.
Similar Classification Devices (HBE)
Other Devices by PHASOR HEALTH LLC
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