← Back to catalogue

Olympus

FDA UDI

Class II (US FDA UDI)

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Olympus FDA UDI
Generic Name
Rigid video laparoscope FDA UDI
Device Name
Video telescope ENDOEYE 3D 10 mm, 30° FDA UDI
Model / Reference
WA50082A FDA UDI
Description
Video telescope ENDOEYE 3D 10 mm, 30° FDA UDI

Identifiers

Catalog Number
WA50082A FDA UDI
Primary DI / UDI-DI
04042761083492 FDA UDI
510(k) Number
K193026 FDA UDI
FDA Product Code
GCM FDA UDI
NWB FDA UDI
FET FDA UDI
GCJ FDA UDI
HET FDA UDI
GMDN Term
Rigid video laparoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
884.1720 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid video laparoscope

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

Similar devices

Also classified as Rigid video laparoscope.

Cleared under the same submission

K193026 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Olympus Winter & Ibe GmbH

Sources (1)

  • FDA UDI d075b596-af77-4c97-be25-daf4504bd045 36 fields · synced May 31, 2026