MultiCup™ - MultiCup Trial Inlay 48 mm/ Innerdia 32 mm - Merete GmbH

Duns Number:313267265

Device Description: MultiCup Trial Inlay 48 mm/ Innerdia 32 mm Standard without rim (for Cups 58/62 mm) non-st MultiCup Trial Inlay 48 mm/ Innerdia 32 mm Standard without rim (for Cups 58/62 mm) non-sterile

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More Product Details

Catalog Number

-

Brand Name

MultiCup™

Version/Model Number

HF84832

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 01, 2021

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

HWT

Product Code Name

TEMPLATE

Device Record Status

Public Device Record Key

7cefdb27-efdd-4399-bf95-a7e614c97840

Public Version Date

November 09, 2021

Public Version Number

1

DI Record Publish Date

November 01, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MERETE GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 328
2 A medical device with a moderate to high risk that requires special controls. 1327
U Unclassified 13