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EC9-4 Transducer

FDA UDI

Class II (US FDA UDI)

by Siemens Medical Solutions Usa, Inc.

Identity

Trade Name
EC9-4 Transducer FDA UDI
Generic Name
Rectal/vaginal ultrasound imaging transducer FDA UDI
Model / Reference
11286590 FDA UDI

Identifiers

Primary DI / UDI-DI
04056869053950 FDA UDI
510(k) Number
K121646 FDA UDI
K121699 FDA UDI
K141846 FDA UDI
K173957 FDA UDI
K173981 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Rectal/vaginal ultrasound imaging transducer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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

No

FDA UDI

Category: Rectal/vaginal ultrasound imaging transducer

EC9-4 Transducer by Siemens Medical Solutions Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rectal/vaginal ultrasound imaging transducer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78cb60fc-ac43-4251-a6b7-9530f460703f 34 fields · synced Jun 8, 2026