Olympus

FDA UDI

Class II (US FDA UDI)

by Olympus Winter & Ibe GmbH

Identity

Trade Name: Olympus FDA UDI
Generic Name: Endoscope suction valve, reusable FDA UDI
Device Name: Sealing cap, blue, for Luer-lock, 6 pcs. FDA UDI
Model / Reference: A0400 FDA UDI
Description: Sealing cap, blue, for Luer-lock, 6 pcs. FDA UDI

Identifiers

Catalog Number: A0400 FDA UDI
Primary DI / UDI-DI: 14042761001707 FDA UDI
FDA Product Code: GCP FDA UDI
GEI FDA UDI
GCJ FDA UDI
HET FDA UDI
FGA FDA UDI
FGB FDA UDI
GMDN Term: Endoscope suction valve, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
878.4400 FDA UDI
884.1720 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope suction valve, reusable

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

Similar devices

Also classified as Endoscope suction valve, reusable.

EM — Allied Medical LLC · Class I
Suction valve — Olympus Medical Systems Corporation · Class II
DUFNER Instrumente GmbH — DUFNER - Instrumente GmbH Fabrik ärztlicher Instrumente Medizintechnik · Class II
DUFNER Instrumente GmbH — DUFNER - Instrumente GmbH Fabrik ärztlicher Instrumente Medizintechnik · Class II
SUCTION VALVE — Olympus Medical Systems Corporation · Class II
SUCTION VALVE — Olympus Medical Systems Corporation · Class II
FUJIFILM — FUJIFILM Corporation · Class I
PENTAX — HOYA CORPORATION · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Olympus Winter & Ibe GmbH

Sources (1)

FDA UDI 7754019b-8910-44b7-9a46-6c30621b292e 35 fields · synced May 30, 2026