NA - ELECTROBLADE GENERATOR ADAPTER - Smith & Nephew, Inc.

Duns Number:109903521

Device Description: ELECTROBLADE GENERATOR ADAPTER REQUIRED TO OPERATE 7205 ELECTROBLADE GENERATOR ADAPTER REQUIRED TO OPERATE 7205962, PACKAGED NON-STERILE, REUSABLE

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More Product Details

Catalog Number

7210380

Brand Name

NA

Version/Model Number

7210380

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

GEI

Product Code Name

ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Device Record Status

Public Device Record Key

03eefeec-a468-4a15-8984-e6023092ea96

Public Version Date

November 03, 2020

Public Version Number

5

DI Record Publish Date

August 30, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SMITH & NEPHEW, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 10651
2 A medical device with a moderate to high risk that requires special controls. 35590
3 A medical device with high risk that requires premarket approval 351