Duns Number:006254430
Device Description: UHMWPE #2 Suture
Catalog Number
-
Brand Name
RoG Rope
Version/Model Number
10-1341
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K113299,K113299
Product Code
MBI
Product Code Name
Fastener, Fixation, Nondegradable, Soft Tissue
Public Device Record Key
37c8dd3e-e570-498a-8408-9a5194d230c3
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
June 13, 2018
Package DI Number
10855152006038
Quantity per Package
10
Contains DI Package
00855152006031
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 3 |