MICRON II MODULAR PORP CENTERED - "70142002 MICRON II MODULAR PORP CENTERE" - Gyrus Acmi, Inc.

Duns Number:007198742

Device Description: "70142002 MICRON II MODULAR PORP CENTERE"

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More Product Details

Catalog Number

-

Brand Name

MICRON II MODULAR PORP CENTERED

Version/Model Number

70142002

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 04, 2018

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

K002737

Product Code Details

Product Code

ETA

Product Code Name

REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL

Device Record Status

Public Device Record Key

b95e7451-ab87-4b25-a455-371172383130

Public Version Date

October 06, 2022

Public Version Number

4

DI Record Publish Date

October 12, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"GYRUS ACMI, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 899
2 A medical device with a moderate to high risk that requires special controls. 1586
3 A medical device with high risk that requires premarket approval 9
U Unclassified 4