← Back to catalogue

Fujifilm

FDA UDI

Class I (US FDA UDI)

by FUJIFILM Corporation

Identity

Trade Name
FUJIFILM FDA UDI
Generic Name
Flexible ultrasound bronchoscope FDA UDI
Device Name
This product is the cleaning adapter used in combination with our endoscopes in medical facilities. Do not use this product for any other purpose. FDA UDI
Model / Reference
CA-500BU FDA UDI
Description
This product is the cleaning adapter used in combination with our endoscopes in medical facilities. Do not use this product for any other purpose. FDA UDI

Identifiers

Primary DI / UDI-DI
04547410104349 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible ultrasound bronchoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible ultrasound bronchoscope

Fujifilm by FUJIFILM Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible ultrasound bronchoscope.

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

Sources (1)

  • FDA UDI c93d528a-8717-486b-8391-73d3a18e13c4 35 fields · synced May 30, 2026