AESCULAP - Bottom, with base perforation, Standard 1/1, - Aesculap AG

Duns Number:315018218

Device Description: Bottom, with base perforation, Standard 1/1, outer length: 592 mm, outer width: 274 mm, ou Bottom, with base perforation, Standard 1/1, outer length: 592 mm, outer width: 274 mm, outer heigth: 135 mm, inner length: 544 mm,inner width: 258 mm, inner heigth: 120 mm

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More Product Details

Catalog Number

JN442

Brand Name

AESCULAP

Version/Model Number

JN442

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

FLE

Product Code Name

Sterilizer, steam

Device Record Status

Public Device Record Key

01a2a379-56a2-4f40-9ca0-83fe34becc2d

Public Version Date

July 08, 2021

Public Version Number

9

DI Record Publish Date

September 23, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AESCULAP AG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 11840
2 A medical device with a moderate to high risk that requires special controls. 7088
3 A medical device with high risk that requires premarket approval 37