← Back to catalogue

Triple Transducer Connect

EUDAMEDFDA UDI

Class I (EU MDR)

Ref P30373-01Model TRIPLE TRANSDUCER CONNECT

by Fujifilm Sonosite, Inc.

Identity

Trade Name
Triple Transducer Connect EUDAMEDFDA UDI
Generic Name
Ultrasound imaging system multi-transducer connection unit FDA UDI
Device Name
TRIPLE TRANSDUCER CONNECT EUDAMED
Diagnostic Ultrasound System Accessory FDA UDI
Model / Reference
TRIPLE TRANSDUCER CONNECT EUDAMED
P30373-01 EUDAMEDFDA UDI
Description
Diagnostic Ultrasound System Accessory FDA UDI

Identifiers

Catalog Number
P30373 FDA UDI
Primary DI / UDI-DI
00841517108090 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517108090 EUDAMED
510(k) Number
K130173 FDA UDI
K162045 FDA UDI
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
OIJ FDA UDI
EMDN Code
Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
GMDN Term
Ultrasound imaging system multi-transducer connection unit 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 889c11a0-84fc-4bfd-85de-7e160091d85d 61 fields · synced Jul 30, 2026
  • FDA UDI 978ac0fd-4580-4d27-9c5a-bfe69a0ab897 36 fields · synced May 30, 2026