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Evis Exera Iii Bronchovideoscope

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
EVIS EXERA III BRONCHOVIDEOSCOPE FDA UDI
Generic Name
Flexible video bronchoscope, reusable FDA UDI
Device Name
BF-Q190 EEIII Q-IMAGE DIAGNOST IC BRONCH FDA UDI
Model / Reference
OLYMPUS BF-Q190 FDA UDI
Description
BF-Q190 EEIII Q-IMAGE DIAGNOST IC BRONCH FDA UDI

Identifiers

Primary DI / UDI-DI
04953170335198 FDA UDI
510(k) Number
K121959 FDA UDI
FDA Product Code
NWB FDA UDI
EOQ FDA UDI
GMDN Term
Flexible video bronchoscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
874.4680 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: Flexible video bronchoscope, reusable

Evis Exera Iii Bronchovideoscope by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video bronchoscope, reusable.

Cleared under the same submission

K121959 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 c44ecf12-f454-49a1-9158-8deb50980ab0 35 fields · synced Jun 1, 2026