Duns Number:246113039
Device Description: VWR S/S 5.25"x10" (1200)
Catalog Number
-
Brand Name
VWR
Version/Model Number
VWR89140800
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K953829,K953829,K953829
Product Code
KCT
Product Code Name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Public Device Record Key
74ab2e7e-7b05-4e78-a726-671e76f56cce
Public Version Date
November 08, 2019
Public Version Number
4
DI Record Publish Date
February 07, 2017
Package DI Number
D830VWR891408002
Quantity per Package
1200
Contains DI Package
D830VWR891408001
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CARDBOARD BOX
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 51 |