Duns Number:832637081
Device Description: PIPE BENDERS WITH LONG HANDLES
Catalog Number
03622060
Brand Name
NA
Version/Model Number
03.622.060
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 20, 2017
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
HXW
Product Code Name
BENDER
Public Device Record Key
8760fcf6-9fee-4e6a-8aee-1d499071c74d
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
December 31, 2016
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 | 1194 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4171 |
| 3 | A medical device with high risk that requires premarket approval | 30 |
| U | Unclassified | 1 |