KAYE FACE LIFT SCISSORS - KAYE FACE LIFT SCISSORS SPATULATED TUNGSTEN - SONTEC INSTRUMENTS, INC.

Duns Number:040729840

Device Description: KAYE FACE LIFT SCISSORS SPATULATED TUNGSTEN CARBIDE POWER CUT CURVED BLUNT BLADE SPREAD HA KAYE FACE LIFT SCISSORS SPATULATED TUNGSTEN CARBIDE POWER CUT CURVED BLUNT BLADE SPREAD HANDLE

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More Product Details

Catalog Number

1200-078

Brand Name

KAYE FACE LIFT SCISSORS

Version/Model Number

1200-078

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)

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

KBD

Product Code Name

Scissors, Nasal

Device Record Status

Public Device Record Key

f2019a14-15e9-4803-8ff1-4de9616898b2

Public Version Date

October 04, 2019

Public Version Number

3

DI Record Publish Date

September 21, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SONTEC INSTRUMENTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 10108
2 A medical device with a moderate to high risk that requires special controls. 3414