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Ultrasonic Probe

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
ULTRASONIC PROBE FDA UDI
Generic Name
Flexible endoscopic ultrasound imaging transducer FDA UDI
Device Name
"UM-S20-20R-3 ULTRASONIC PROBE" FDA UDI
Model / Reference
UM-S20-20R FDA UDI
Description
"UM-S20-20R-3 ULTRASONIC PROBE" FDA UDI

Identifiers

Primary DI / UDI-DI
04953170368592 FDA UDI
510(k) Number
K001203 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Flexible endoscopic 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

Yes

FDA UDI

Category: Flexible endoscopic ultrasound imaging transducer

Ultrasonic Probe by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic ultrasound imaging transducer.

Cleared under the same submission

K001203 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI a193828f-b8de-42cc-b187-13e34cced1a4 35 fields · synced May 30, 2026