Duns Number:080935429
Device Description: Anti-Embolism Stockings,Thigh Length,X-Large,Short,Size K
Catalog Number
4010LF
Brand Name
T.E.D.
Version/Model Number
4010LF
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
July 01, 2023
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
-
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
DWL
Product Code Name
Stocking, medical support (to prevent pooling of blood in legs)
Public Device Record Key
9f34a465-4897-40d6-9a0f-e2e863ce8629
Public Version Date
December 17, 2020
Public Version Number
8
DI Record Publish Date
September 24, 2016
Package DI Number
20884521025216
Quantity per Package
36
Contains DI Package
00884521025212
Package Discontinue Date
July 01, 2023
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 | 672 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
| U | Unclassified | 17 |