FUJIFILM - This product is intended for use, under the - FUJIFILM CORPORATION

Duns Number:713565195

Device Description: This product is intended for use, under the management of physicians in medical facilities This product is intended for use, under the management of physicians in medical facilities, as a water tank connected to a FUJIFILM or FUJINON Endoscope which can supply water when used in combination with an endoscopic processor or light source.

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More Product Details

Catalog Number

-

Brand Name

FUJIFILM

Version/Model Number

WT-4

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FDS

Product Code Name

Gastroscope and accessories, flexible/rigid

Device Record Status

Public Device Record Key

9ed3f414-22a7-42c4-8c34-13451a6522c4

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 16, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FUJIFILM CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 43
2 A medical device with a moderate to high risk that requires special controls. 324
3 A medical device with high risk that requires premarket approval 1