← Back to catalogue

Video Coupler

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Video Coupler FDA UDI
Generic Name
Electrical mains power cable FDA UDI
Device Name
"MH-999E COUPLER OTV-S5 EYEPIEC" FDA UDI
Model / Reference
OLYMPUS MH-999E FDA UDI
Description
"MH-999E COUPLER OTV-S5 EYEPIEC" FDA UDI

Identifiers

Catalog Number
5705130 FDA UDI
Primary DI / UDI-DI
04953170028465 FDA UDI
FDA Product Code
GCJ FDA UDI
EOQ FDA UDI
FAJ FDA UDI
KNS FDA UDI
KGE FDA UDI
FDS FDA UDI
EOB FDA UDI
FCL FDA UDI
FGB FDA UDI
FGA FDA UDI
FDI FDA UDI
HET FDA UDI
FDF FDA UDI
NWB FDA UDI
GMDN Term
Electrical mains power cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
874.4680 FDA UDI
876.4300 FDA UDI
874.4760 FDA UDI
876.1075 FDA UDI
884.1720 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Video Coupler by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 Medical Systems Corporation

Sources (1)

  • FDA UDI c261bed8-2e65-4c0d-9bf4-eba2a1c8eef2 36 fields · synced Jun 6, 2026