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Extension Unit For Uces-4

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
EXTENSION UNIT FOR UCES-4 FDA UDI
Generic Name
Electrical-only medical device connection adaptor, reusable FDA UDI
Device Name
EXTENSION UNIT FOR UCES-4 FDA UDI
Model / Reference
MAJ-2191 FDA UDI
Description
EXTENSION UNIT FOR UCES-4 FDA UDI

Identifiers

Primary DI / UDI-DI
04953170391804 FDA UDI
510(k) Number
K172618 FDA UDI
FDA Product Code
GCJ FDA UDI
ODA FDA UDI
GMDN Term
Electrical-only medical device connection adaptor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

Extension Unit For Uces-4 by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K172618 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI 4cde5af5-cbda-42df-b492-901b42393952 36 fields · synced Jun 6, 2026