Duns Number:198227881
Device Description: H3+ 3-channel digital Holter Recorder - 7-day, includes carry case with clip, and hookup k H3+ 3-channel digital Holter Recorder - 7-day, includes carry case with clip, and hookup kit (not available for US); Italian language and CD manual; IEC 5 wire, 15 inch (38cm), LeadForm patient cable with snap ends
Catalog Number
H3PLUS-CEE-XXXXX
Brand Name
Welch Allyn, Inc.
Version/Model Number
901142
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MWJ
Product Code Name
Electrocardiograph, ambulatory (without analysis)
Public Device Record Key
a70c82c5-e3f5-4775-ad3d-123e5b997c2a
Public Version Date
June 28, 2022
Public Version Number
3
DI Record Publish Date
July 01, 2019
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 |