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Ultrasonic Transducer

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref X9007620Model Senhance Ultrasonic Surgical System

by Asensus Surgical Italia S.r.l.

Identity

Trade Name
Ultrasonic Transducer EUDAMED
Senhance Ultrasonic FDA UDI
Generic Name
Soft-tissue ultrasonic surgical system transducer/tip FDA UDI
Device Name
Ultrasonic Transducer EUDAMED
Senhance Ultrasonic Transducer FDA UDI
Model / Reference
Senhance Ultrasonic Surgical System EUDAMED
X9007620 EUDAMEDFDA UDI
Description
Senhance Ultrasonic Transducer FDA UDI

Identifiers

Catalog Number
300-11011 FDA UDI
Primary DI / UDI-DI
00815440021573 EUDAMEDFDA UDI
Basic UDI-DI
081544002TD003BQ8 EUDAMED
Direct Marketing DI
00815440021573 EUDAMED
510(k) Number
K182421 FDA UDI
FDA Product Code
NAY FDA UDI
EMDN Code
L1306 ULTRASONIC GENERATOR ROBOTIC SURGERY INSTRUMENTS, REUSABLE EUDAMED
GMDN Term
Soft-tissue ultrasonic surgical system transducer/tip FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Ultrasonic Transducer by Asensus Surgical Italia S.r.l. — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
IT-MF-000007964

Sources (2)

  • EUDAMED 15fdccb5-e6c6-4c58-a221-3d22d53cc1b0 61 fields · synced Jun 20, 2026
  • FDA UDI 4bfd182c-1b7e-4c7f-9bd6-5374d141ac5f 35 fields · synced May 30, 2026