gudid
Primary ID: 2-IN-1-45K
PHASOR (UDI 2-IN-1-45K)
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 2-IN-1-45K
Device Regulatory Overview
The PHASOR (Model/Catalog Number: 2-IN-1-45K) 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
- 2-IN-1-45K
- Product Code / EMDN
- HBE
- Device Name
- The Phasor Drill is a sterile, single-use, disposable device intended for use on adult patients during neurosurgical procedures for drilling of cranial and orthopedic bone, with interchangeable quick-connect, 2 bits (diameters 4.50-mm, 5.30-mm) with Kit.
- Database Sync Date
- 2026-08-09 09:06:29
Full Regulatory Attributes
🔒 Token Gated
{
"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 2-IN-1-45K.
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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