STERI-SOX MULTI-CHANNEL STERILIZATION POUCHES - MAXILL, INC.

Duns Number:079343581

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More Product Details

Catalog Number

-

Brand Name

STERI-SOX MULTI-CHANNEL STERILIZATION POUCHES

Version/Model Number

6070560149

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K202462,K202462,K202462

Product Code Details

Product Code

FRG

Product Code Name

Wrap, Sterilization

Device Record Status

Public Device Record Key

25a09078-0146-4a38-aec7-43b87f4eccb8

Public Version Date

September 27, 2022

Public Version Number

1

DI Record Publish Date

September 19, 2022

Additional Identifiers

Package DI Number

D89260705601492

Quantity per Package

2000

Contains DI Package

D89260705601491

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"MAXILL, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 208
2 A medical device with a moderate to high risk that requires special controls. 61