Duns Number:144796497
Device Description: 133P-SX-14
Catalog Number
133P-SX-14
Brand Name
Natrelle 133 Plus Tissue Expanders
Version/Model Number
133P-SX-14
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 24, 2019
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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
-
Product Code
LCJ
Product Code Name
Expander, Skin, Inflatable
Public Device Record Key
b2804c55-5e13-4a23-b126-7a1faf6f83a2
Public Version Date
October 15, 2021
Public Version Number
3
DI Record Publish Date
March 21, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 3 |
3 | A medical device with high risk that requires premarket approval | 982 |
U | Unclassified | 702 |