Duns Number:014464314
Device Description: Sheet 90cmx90cm Kit Pack Fold
Catalog Number
E2739KPFN
Brand Name
Exact Medical Manufacturing
Version/Model Number
E2739KPFN
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"
Yes
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
K101598,K101598
Product Code
KKX
Product Code Name
Drape, Surgical
Public Device Record Key
1cf0f054-b83c-4958-871e-b78b9608479c
Public Version Date
December 22, 2021
Public Version Number
2
DI Record Publish Date
October 06, 2021
Package DI Number
00850033380521
Quantity per Package
200
Contains DI Package
00850033380514
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 3 |
2 | A medical device with a moderate to high risk that requires special controls. | 489 |