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Exablate Neuro Treatment Accessories Kit

FDA UDI

Class III (US FDA UDI)

by Insightec

Identity

Trade Name
Exablate Neuro Treatment Accessories Kit FDA UDI
Generic Name
Ultrasonic hyperthermia system FDA UDI
Device Name
Exablate Neuro Treatment Accessories Kit FDA UDI
Model / Reference
Exablate 4000 FDA UDI
Description
Exablate Neuro Treatment Accessories Kit FDA UDI

Identifiers

Catalog Number
SET004307-ROW FDA UDI
Primary DI / UDI-DI
07290019402565 FDA UDI
PMA Number
P150038 FDA UDI
FDA Product Code
POH FDA UDI
GMDN Term
Ultrasonic hyperthermia system FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Category: Ultrasonic hyperthermia system

Exablate Neuro Treatment Accessories Kit by Insightec — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic hyperthermia system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Insightec

Sources (1)

  • FDA UDI d63dffdb-2044-4114-87db-d300c06f1144 37 fields · synced May 31, 2026