FUJIFILM - This product is exclusively used for manual - FUJIFILM CORPORATION

Duns Number:713565195

Device Description: This product is exclusively used for manual cleaning and manual disinfection of a FUJIFILM This product is exclusively used for manual cleaning and manual disinfection of a FUJIFILM endoscope in medical facilities.Do not use this product for any other purpose.

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More Product Details

Catalog Number

-

Brand Name

FUJIFILM

Version/Model Number

CA-606

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)

Yes

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

FFY

Product Code Name

Adaptor, bulbs, miscellaneous, for endoscope

Device Record Status

Public Device Record Key

05ce2091-f319-44e2-b7ca-ce2894cf7b96

Public Version Date

October 17, 2022

Public Version Number

1

DI Record Publish Date

October 07, 2022

Additional Identifiers

Package DI Number

24547410245343

Quantity per Package

1

Contains DI Package

04547410245349

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"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