SUCTION TUBE - SUCTION TUBE BASE - MIZUHO CORPORATION

Duns Number:690677802

Device Description: SUCTION TUBE BASE

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More Product Details

Catalog Number

07-960-18

Brand Name

SUCTION TUBE

Version/Model Number

07-960-18

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

HAO

Product Code Name

Instrument, Surgical, Non-Powered

Device Record Status

Public Device Record Key

124f89e6-5857-4b49-8c26-6437b1a6456d

Public Version Date

April 22, 2022

Public Version Number

1

DI Record Publish Date

April 14, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MIZUHO CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 696
2 A medical device with a moderate to high risk that requires special controls. 566