← Back to catalogue

Olympus

FDA UDI

Class II (US FDA UDI)

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Olympus FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Device Name
Sealing cap, 0.1 mm, 6 pieces FDA UDI
Model / Reference
A0298 FDA UDI
Description
Sealing cap, 0.1 mm, 6 pieces FDA UDI

Identifiers

Catalog Number
A0298 FDA UDI
Primary DI / UDI-DI
14042761001363 FDA UDI
FDA Product Code
GCP FDA UDI
GMDN Term
Endoscope working-channel valve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope working-channel valve, single-use

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

Similar devices

Also classified as Endoscope working-channel valve, single-use.

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

Sources (1)

  • FDA UDI 2af53bb7-5b15-4a4f-9ec6-fdfa121525a2 35 fields · synced May 31, 2026