← Back to catalogue

Visera S Video System Center

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
VISERA S VIDEO SYSTEM CENTER FDA UDI
Generic Name
Endoscopic video image processing/light source system FDA UDI
Model / Reference
OLYMPUS OTV-S500 FDA UDI

Identifiers

Catalog Number
N6214840 FDA UDI
Primary DI / UDI-DI
04953170454141 FDA UDI
FDA Product Code
NTN FDA UDI
NWB FDA UDI
EOB FDA UDI
EOQ FDA UDI
EQL FDA UDI
HET FDA UDI
GMDN Term
Endoscopic video image processing/light source system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
874.4760 FDA UDI
874.4680 FDA UDI
874.4750 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

Category: Endoscopic video image processing/light source system

Visera S Video System Center by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing/light source system.

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 4a666fea-32b8-4367-b638-55526a438cd3 34 fields · synced May 29, 2026