n/a - 1410 W/A-INH & EXH, B-MTHPRT - HANS RUDOLPH, INC.

Duns Number:007131725

Device Description: 1410 W/A-INH & EXH, B-MTHPRT

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More Product Details

Catalog Number

C119

Brand Name

n/a

Version/Model Number

1410

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

CBP

Product Code Name

Valve, Non-Rebreathing

Device Record Status

Public Device Record Key

db385205-6045-485b-929f-11125ecf361c

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 16, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HANS RUDOLPH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 922
2 A medical device with a moderate to high risk that requires special controls. 407