Duns Number:070556204
Device Description: *Custom* Curaplex New Jersey OB Kit
Catalog Number
8600-01461
Brand Name
Curaplex
Version/Model Number
8600-01461
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
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OKU
Product Code Name
Emergency obstetrical kit
Public Device Record Key
aed481f5-790c-424e-be33-eed0c903dc6d
Public Version Date
August 16, 2022
Public Version Number
2
DI Record Publish Date
November 30, 2020
Package DI Number
00810094572471
Quantity per Package
35
Contains DI Package
00812277036596
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CS
| 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 |