Mepitel® Film - Mepitel Film 10x12cm - Mölnlycke Health Care AB

Duns Number:631770658

Device Description: Mepitel Film 10x12cm

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More Product Details

Catalog Number

-

Brand Name

Mepitel® Film

Version/Model Number

296270

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)

-

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

NAD

Product Code Name

Dressing, wound, occlusive

Device Record Status

Public Device Record Key

11ba428a-1389-4a3f-818b-9940ea233a14

Public Version Date

October 31, 2022

Public Version Number

1

DI Record Publish Date

October 21, 2022

Additional Identifiers

Package DI Number

07323190262991

Quantity per Package

10

Contains DI Package

07332551974350

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

PACK_OR_INNER_PACK

"MÖLNLYCKE HEALTH CARE AB" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 212
2 A medical device with a moderate to high risk that requires special controls. 15
U Unclassified 18