PowerSuture Tape

GUDID 10810020084440

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament
Primary Device ID10810020084440
NIH Device Record Keya768873a-e4f0-4ea4-b6c4-a34f73e13e88
Commercial Distribution StatusIn Commercial Distribution
Brand NamePowerSuture Tape
Version Model Number05.03.0151
Company DUNS964053560
Company NameRIVERPOINT MEDICAL, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810020084443 [Primary]
GS110810020084440 [Package]
Contains: 00810020084443
Package: [12 Units]
In Commercial Distribution

FDA Product Code

GATSuture, Nonabsorbable, Synthetic, Polyethylene

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-04-20
Device Publish Date2021-04-12

On-Brand Devices [PowerSuture Tape]

10810020084532Suture
10810020084525Suture
10810020084518Suture
10810020084471Suture
10810020084464Suture
10810020084457Suture
10810020084440Suture
10810020084433Suture
10810020084426Suture
10810020084419Suture
10810020084402Suture
10840277404395Meniscal Needles – Double Armed, Black Braided UHMWPE Non-Absorbable Suture
10840277404388Meniscal Needles – Single Armed, Black Braided UHMWPE Non-Absorbable Suture

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.