Duns Number:565751992
Device Description: Tyvek Pouch 10cm x 30cm
Catalog Number
61301606737
Brand Name
Getinge Pack Tyvek Pouch
Version/Model Number
GUTP1030
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
K160595,K160595,K160595
Product Code
FRG
Product Code Name
Wrap, Sterilization
Public Device Record Key
2c893f5b-265e-4b23-953c-9a5518b73446
Public Version Date
November 08, 2019
Public Version Number
5
DI Record Publish Date
September 26, 2017
Package DI Number
10850144008137
Quantity per Package
4
Contains DI Package
00850144008130
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 6 |