NOVA Lite® Monkey Oesophagus IFA Kit - 1. 10 x Monkey Oesophagus – 5-well slide2. 1 x - INOVA DIAGNOSTICS, INC.

Duns Number:188354831

Device Description: 1. 10 x Monkey Oesophagus – 5-well slide2. 1 x 1mL Pemphigus Positive Control (prediluted) 1. 10 x Monkey Oesophagus – 5-well slide2. 1 x 1mL Pemphigus Positive Control (prediluted)3. 1 x 1mL Endomysial (Celiac) Positive Control (prediluted)4. 1 x 1mL IFA System Negative Control (prediluted)5. 1 x 7mL FITC IgG (H&L), monkey adsorbed Conjugate6. 1 x 7mL Anti-Human IgA (α) AFF FITC7. 1 x 3mL 1% Evans Blue Counterstain8. 2 x 25mL PBS II concentrate (x40)9. 1 x 3mL Mounting Medium10. 10 x Coverslips 11. 1 x instruction leaflet

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More Product Details

Catalog Number

-

Brand Name

NOVA Lite® Monkey Oesophagus IFA Kit

Version/Model Number

704145

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

K981209

Product Code Details

Product Code

MVM

Product Code Name

Autoantibodies, Endomysial(Tissue Transglutaminase)

Device Record Status

Public Device Record Key

a12a808d-ee71-4a05-90b4-a8b7515c76c7

Public Version Date

January 08, 2019

Public Version Number

4

DI Record Publish Date

August 31, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INOVA DIAGNOSTICS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 36
2 A medical device with a moderate to high risk that requires special controls. 215