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ExAblate 2100/2100V1/2100V1-AR UPPER PELVIC COIL

FDA UDI

Class III (US FDA UDI)

by Insightec

Identity

Trade Name
ExAblate 2100/2100V1/2100V1-AR UPPER PELVIC COIL FDA UDI
Generic Name
Therapeutic oncological/gynaecological ultrasound system FDA UDI
Device Name
ExAblate 2100/2100V1/2100V1-AR UPPER PELVIC COIL for MRI imaging during Body FUS treatments. Contains Upper and Lower part: FDA UDI
Model / Reference
ASM000426-AA ExAblate 2100/2100V1/2100V1-AR UPPER PELVIC COIL FDA UDI
Description
ExAblate 2100/2100V1/2100V1-AR UPPER PELVIC COIL for MRI imaging during Body FUS treatments. Contains Upper and Lower part: FDA UDI

Identifiers

Catalog Number
ASM000426-AA FDA UDI
Primary DI / UDI-DI
07290015461504 FDA UDI
FDA Product Code
NRZ FDA UDI
LSY FDA UDI
GMDN Term
Therapeutic oncological/gynaecological ultrasound 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Therapeutic oncological/gynaecological ultrasound system

ExAblate 2100/2100V1/2100V1-AR UPPER PELVIC COIL by Insightec — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic oncological/gynaecological ultrasound system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Insightec

Sources (1)

  • FDA UDI 981eb018-8c2f-40ad-aae3-b97b149cd45c 36 fields · synced Jun 1, 2026