Duns Number:070556204
Device Description: Curaplex Select Multi-Function Defib Pads, Physio-Control Pediatric 10pr/cs
Catalog Number
-
Brand Name
Curaplex
Version/Model Number
16383
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"
Yes
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
K081442,K081442
Product Code
LDD
Product Code Name
Dc-defibrillator, low-energy, (including paddles)
Public Device Record Key
36a3dae9-7b18-4fa4-87a4-608bc0cf0b35
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
December 14, 2016
Package DI Number
00815277023924
Quantity per Package
10
Contains DI Package
00815277023917
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 471 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 540 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 1 |