POTENZA Tip - C21-1 Tip (FDA/1EA) - Jeisys Medical Inc.

Duns Number:690275362

Device Description: C21-1 Tip (FDA/1EA)

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More Product Details

Catalog Number

-

Brand Name

POTENZA Tip

Version/Model Number

C21-1 Tip

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

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

K201685,K201685

Product Code Details

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Device Record Status

Public Device Record Key

c32f0fc9-67cd-4e34-8494-c0b9f71236b8

Public Version Date

April 06, 2022

Public Version Number

1

DI Record Publish Date

March 29, 2022

Additional Identifiers

Package DI Number

18800020101157

Quantity per Package

5

Contains DI Package

08800020101150

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CARTON BOX

"JEISYS MEDICAL INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2
2 A medical device with a moderate to high risk that requires special controls. 36