Duns Number:604056226
Device Description: Sterilization Wrap, 500 Weight, 30-inch x 30-inch, 90 day
Catalog Number
WR500-30-30
Brand Name
NA
Version/Model Number
WR500-30-30
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K160755,K171533,K160755,K171533
Product Code
FRG
Product Code Name
Wrap, sterilization
Public Device Record Key
f36aacd7-490d-45d9-8525-cd1cbc39a030
Public Version Date
May 11, 2022
Public Version Number
2
DI Record Publish Date
April 08, 2022
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 | 326 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 219 |