CODMAN - CODMAN Disposable ICP Kit, Plastic, Adult - CODMAN & SHURTLEFF, INC.

Duns Number:607846297

Device Description: CODMAN Disposable ICP Kit, Plastic, Adult CONTENTS: 1 ICP Screw, 2 Spacing Washers, 1 Hand CODMAN Disposable ICP Kit, Plastic, Adult CONTENTS: 1 ICP Screw, 2 Spacing Washers, 1 Handle 1 Retractor, 1 5cc Syringe with 22ga x 1.5 Inches, 1 Drill Assembly 1 Obturator, 1 18ga Spinal Needle 3 Inches, 1 1cc Syringe with 25ga x 5/8 Inch 1 Allen Wrench, 2 Disposable Forceps, 2 Drapes (18 Inches x 26 Inches) 8 4 x 4 Gauze, 1 Bone Wax 2.5gms, 1 Male Luer Lock Cap 1 Number 15 Disposable Scalpel, 1 Fenestrated Drape (24 Inches x 26 Inches)

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More Product Details

Catalog Number

801196

Brand Name

CODMAN

Version/Model Number

80-1196

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 01, 2022

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

K853770

Product Code Details

Product Code

GWM

Product Code Name

DEVICE, MONITORING, INTRACRANIAL PRESSURE

Device Record Status

Public Device Record Key

6ad7bfff-8ea0-467e-8568-a69d70a11d2b

Public Version Date

September 01, 2022

Public Version Number

5

DI Record Publish Date

June 30, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CODMAN & SHURTLEFF, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 40
2 A medical device with a moderate to high risk that requires special controls. 1054
3 A medical device with high risk that requires premarket approval 11