RAN-1115 #0016008 - RAN-1115 Customer #0016008PN 74285-02M - RANFAC CORP.

Duns Number:121622872

Device Description: RAN-1115 Customer #0016008PN 74285-02M

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More Product Details

Catalog Number

74285-02M

Brand Name

RAN-1115 #0016008

Version/Model Number

11 Gauge x 15 CM

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"

Yes

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

K131157,K131157,K131157

Product Code Details

Product Code

KNW

Product Code Name

Instrument, Biopsy

Device Record Status

Public Device Record Key

58a801a2-7ef7-46b0-bfef-9ad3c1605ed6

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 09, 2017

Additional Identifiers

Package DI Number

20858690006031

Quantity per Package

10

Contains DI Package

10858690006034

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"RANFAC CORP." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 31
2 A medical device with a moderate to high risk that requires special controls. 93