Duns Number:198227881
Device Description: Welch Allyn Spirometer Upgrade for CP 200 Electrocardiograph, includes? Serial Port Adapte Welch Allyn Spirometer Upgrade for CP 200 Electrocardiograph, includes? Serial Port Adapter / Sensor ?Handle, Pressure Tubing with Connectors, Nose Clip, 4 pack of flow transducer tubes, 3 L calibration syringe, and CD
Catalog Number
100400
Brand Name
Welch Allyn, Inc.
Version/Model Number
901049
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
DPS
Product Code Name
ELECTROCARDIOGRAPH
Public Device Record Key
aecfa239-0f40-415a-be15-b0bcb31d4d38
Public Version Date
June 28, 2022
Public Version Number
7
DI Record Publish Date
December 05, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 374 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4080 |
| 3 | A medical device with high risk that requires premarket approval | 1 |