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Sonalleve

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 451000080766Model SONALLEVE MR-HIFU V2 ACHIEVA 1.5TModel SONALLEVE MR-HIFU

by Profound Medical Inc.

Identity

Trade Name
Sonalleve EUDAMEDFDA UDI
SONALLEVE MR-HIFU V2 ACHIEVA 1.5T EUDAMED
Generic Name
Therapeutic oncological/gynaecological ultrasound system FDA UDI
Device Name
Sonalleve MR-HIFU EUDAMED
SONALLEVE MR-HIFU V2 ACHIEVA 1.5T FDA UDI
Model / Reference
SONALLEVE MR-HIFU V2 ACHIEVA 1.5T EUDAMED
451000080766 EUDAMEDFDA UDI
SONALLEVE MR-HIFU EUDAMED
Description
SONALLEVE MR-HIFU V2 ACHIEVA 1.5T FDA UDI

Identifiers

Catalog Number
451000080766 FDA UDI
Primary DI / UDI-DI
07540281000236 EUDAMEDFDA UDI
Basic UDI-DI
B-07540281000236 EUDAMED
75402810200097 EUDAMED
Direct Marketing DI
07540281000236 EUDAMED
PMA Number
H190003 FDA UDI
FDA Product Code
QND FDA UDI
EMDN Code
Z1204021501 MULTI-DISTRICT ONCOLOGICAL HYPERTHERMIA EQUIPMENT EUDAMED
GMDN Term
Therapeutic oncological/gynaecological ultrasound system FDA UDI

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 Conditional FDA UDI

Sonalleve by Profound Medical Inc. — Class IIb — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CA-MF-000028761
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (3)

  • EUDAMED 6b76e543-7b47-466f-a8fd-8b24e3f23bb4 61 fields · synced Jul 24, 2026
  • EUDAMED ad654904-9023-404c-a66d-a1e9b8f18b89 61 fields · synced May 19, 2026
  • FDA UDI 95819ade-5bb6-4e82-92f0-c0df552af3bb 35 fields · synced May 30, 2026