EliA Ro Well - EliA Ro Well - Phadia AB

Duns Number:354019424

Device Description: EliA Ro Well

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More Product Details

Catalog Number

DECC055030

Brand Name

EliA Ro Well

Version/Model Number

DECC055030

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

-

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

K082759,K082759

Product Code Details

Product Code

LKJ

Product Code Name

ANTINUCLEAR ANTIBODY, ANTIGEN, CONTROL

Device Record Status

Public Device Record Key

c20755a3-4844-4e72-be7a-421f8f8a61c0

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 23, 2016

Additional Identifiers

Package DI Number

07333066010588

Quantity per Package

4

Contains DI Package

07333066014548

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