AESCULAP - SPECIALTY DISP FCP 203MM X 76MM X 1.0MM - AESCULAP, INC.

Duns Number:082594540

Device Description: SPECIALTY DISP FCP 203MM X 76MM X 1.0MM

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More Product Details

Catalog Number

US805SU

Brand Name

AESCULAP

Version/Model Number

US805SU

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

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

K900533,K900533

Product Code Details

Product Code

GEI

Product Code Name

ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Device Record Status

Public Device Record Key

ca89d1bd-2670-4ec6-9b2f-c0aff1eeee52

Public Version Date

January 15, 2020

Public Version Number

5

DI Record Publish Date

May 23, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AESCULAP, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3239
2 A medical device with a moderate to high risk that requires special controls. 683