SICAT ACCESSGUIDE - SICAT ACCESSGUIDE - SiCAT GmbH & Co. KG

Duns Number:333707003

Device Description: SICAT ACCESSGUIDE

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More Product Details

Catalog Number

10601

Brand Name

SICAT ACCESSGUIDE

Version/Model Number

10601

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)

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

EJL

Product Code Name

Bur, Dental

Device Record Status

Public Device Record Key

ec8c9ce3-5011-4bae-a08d-548bf48040d8

Public Version Date

August 15, 2022

Public Version Number

1

DI Record Publish Date

August 07, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SICAT GMBH & CO. KG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2
2 A medical device with a moderate to high risk that requires special controls. 20
U Unclassified 1