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Olympus

FDA UDI

Class II (US FDA UDI)

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Olympus FDA UDI
Generic Name
Rigid optical rhinoscope FDA UDI
Device Name
Telescope, 4 mm, 30°, connector for light guide on top, autoclavable FDA UDI
Model / Reference
WA96202A FDA UDI
Description
Telescope, 4 mm, 30°, connector for light guide on top, autoclavable FDA UDI

Identifiers

Catalog Number
WA96202A FDA UDI
Primary DI / UDI-DI
04042761070041 FDA UDI
510(k) Number
K944072 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Rigid optical rhinoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical rhinoscope

Olympus by Olympus Winter & Ibe GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical rhinoscope.

Cleared under the same submission

K944072 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Winter & Ibe GmbH

Sources (1)

  • FDA UDI e4e615fb-a236-44dd-b1d1-47ab368e7ed4 36 fields · synced May 30, 2026