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Phasor

FDA UDI

by Phasor Health, LLC

Identity

Trade Name
PHASOR FDA UDI
Generic Name
Craniotomy power tool system, battery-powered, single-use FDA UDI
Device Name
Phasor Drill 2.70-mm diameter, ~70-mm length with Optional Secondary Drill Stop + Kit (Version A) FDA UDI
Model / Reference
PH-270-70-S + PH-K-A FDA UDI
Description
Phasor Drill 2.70-mm diameter, ~70-mm length with Optional Secondary Drill Stop + Kit (Version A) FDA UDI

Identifiers

Catalog Number
PH-270-70-S + PH-K-A FDA UDI
Primary DI / UDI-DI
B775PH27070SPHKA0 FDA UDI
GMDN Term
Craniotomy power tool system, battery-powered, single-use FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Neurosurgical procedure kit, medicatedCraniotomy power tool system, battery-powered, single-use

Phasor by Phasor Health, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniotomy power tool system, battery-powered, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Phasor Health, LLC

Sources (1)

  • FDA UDI 0c0164a6-d440-4117-8203-d768f3e5da89 35 fields · synced Jun 1, 2026