EliA M2 Positive Control 2500/5000 - EliA M2 Positive Control 2500/5000 - Phadia AB

Duns Number:354019424

Device Description: EliA M2 Positive Control 2500/5000

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More Product Details

Catalog Number

83-0015-01

Brand Name

EliA M2 Positive Control 2500/5000

Version/Model Number

83-0015-01

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

K181556,K181556

Product Code Details

Product Code

DBM

Product Code Name

ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL

Device Record Status

Public Device Record Key

5a8c9dee-98ed-49aa-a4cb-ceaf2a76030a

Public Version Date

December 17, 2020

Public Version Number

1

DI Record Publish Date

December 09, 2020

Additional Identifiers

Package DI Number

07333066014333

Quantity per Package

6

Contains DI Package

07333066013527

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"PHADIA AB" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 225
2 A medical device with a moderate to high risk that requires special controls. 518