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-617

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

7d8ca84e-9ae5-4df3-9fa1-1f7144e634cd

Public Version Date

June 08, 2021

Public Version Number

1

DI Record Publish Date

May 31, 2021

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