I-neb Generic ClinicalStudy Disc Power10 - I-neb Generic Clinical Study Disc Power10 - RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD

Duns Number:220018415

Device Description: I-neb Generic Clinical Study Disc Power10

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More Product Details

Catalog Number

1124498

Brand Name

I-neb Generic ClinicalStudy Disc Power10

Version/Model Number

1124498

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

-

Product Code Details

Product Code

CAF

Product Code Name

Nebulizer (direct patient interface)

Device Record Status

Public Device Record Key

7e156c13-d871-4758-a9e5-75781e9229f6

Public Version Date

April 01, 2020

Public Version Number

1

DI Record Publish Date

March 24, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 10
2 A medical device with a moderate to high risk that requires special controls. 399