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Olympus

FDA UDI

Class II (US FDA UDI)

by SCHÖLLY FIBEROPTIC GmbH

Identity

Trade Name
Olympus FDA UDI
Generic Name
Rigid optical rhinoscope FDA UDI
Device Name
Sinuscope, 4 x 175 mm, 30°, HD, wide angle, autoclavable FDA UDI
Model / Reference
WA96304A FDA UDI
Description
Sinuscope, 4 x 175 mm, 30°, HD, wide angle, autoclavable FDA UDI

Identifiers

Catalog Number
WA96304A FDA UDI
Primary DI / UDI-DI
04250480106822 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 SCHÖLLY FIBEROPTIC GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical rhinoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SCHÖLLY FIBEROPTIC GmbH

Sources (1)

  • FDA UDI b2029366-3924-44bf-b6b7-1a1a9f75f2ea 35 fields · synced Jun 8, 2026