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Triple Transducer Connect

EUDAMEDFDA UDI

Class I (EU MDR)

Ref P16535-04Model TRIPLE TRANSDUCER CONNECT, QUICK RELEASE NON D2 COMPATIBLE

by Fujifilm Sonosite, Inc.

Identity

Trade Name
Triple Transducer Connect EUDAMEDFDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
TRIPLE TRANSDUCER CONNECT, QUICK RELEASE NON D2 COMPATIBLE EUDAMED
Diagnostic Ultrasound System Accessory FDA UDI
Model / Reference
TRIPLE TRANSDUCER CONNECT, QUICK RELEASE NON D2 COMPATIBLE EUDAMED
P16535-04 EUDAMEDFDA UDI
Description
Diagnostic Ultrasound System Accessory FDA UDI

Identifiers

Catalog Number
P16535 FDA UDI
Primary DI / UDI-DI
00841517103941 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517103941 EUDAMED
510(k) Number
K130173 FDA UDI
K133454 FDA UDI
K153626 FDA UDI
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
EMDN Code
Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
GMDN Term
General-purpose ultrasound imaging system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.1550 FDA UDI
892.1560 FDA UDI
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

Triple Transducer Connect by Fujifilm Sonosite, Inc. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

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
US-MF-000001075
Authorised Representative
Fujifilm Sonosite B.V. NL-AR-000000046

Sources (2)

  • EUDAMED 2b6bbceb-0467-4270-96bc-bb0cb0c0a17e 61 fields · synced Aug 3, 2026
  • FDA UDI cb7ea1a7-d178-4a71-810c-d965ac56df07 36 fields · synced May 30, 2026