ETHICON PHYSIOMESH - Physiomesh Open Medium Envelope - Johnson & Johnson International Inc.

Duns Number:372587696

Device Description: Physiomesh Open Medium Envelope

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More Product Details

Catalog Number

OPHY1525

Brand Name

ETHICON PHYSIOMESH

Version/Model Number

OPHY1525

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

-

Product Code Details

Product Code

FTL

Product Code Name

Mesh, surgical, polymeric

Device Record Status

Public Device Record Key

54d30c33-f9f6-4f3a-9615-76c39613b536

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

January 25, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"JOHNSON & JOHNSON INTERNATIONAL INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 84