SONTEC-WECK TROUTMAN CORNEAL DISSECTOR - SONTEC-WECK TROUTMAN CORNEAL DISSECTOR SINGLE - SONTEC INSTRUMENTS, INC.

Duns Number:040729840

Device Description: SONTEC-WECK TROUTMAN CORNEAL DISSECTOR SINGLE ENDED BLADE

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More Product Details

Catalog Number

11-3423

Brand Name

SONTEC-WECK TROUTMAN CORNEAL DISSECTOR

Version/Model Number

11-3423

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

GDI

Product Code Name

Dissector, Surgical, General & Plastic Surgery

Device Record Status

Public Device Record Key

bf0a2891-0305-451e-817d-bd1a534d3f1b

Public Version Date

February 24, 2020

Public Version Number

3

DI Record Publish Date

October 08, 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