Riverlon

GUDID 10810020084020

suture

RIVERPOINT MEDICAL, LLC

Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament Nylon suture, non-bioabsorbable, monofilament
Primary Device ID10810020084020
NIH Device Record Key6126f092-4d93-4e02-acbe-1bb72e21c532
Commercial Distribution StatusIn Commercial Distribution
Brand NameRiverlon
Version Model Number389BK
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
GS100810020084023 [Primary]
GS110810020084020 [Package]
Contains: 00810020084023
Package: [12 Units]
In Commercial Distribution

FDA Product Code

GARSuture, Nonabsorbable, Synthetic, Polyamide

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-29
Device Publish Date2020-07-21

On-Brand Devices [Riverlon]

10812444027126Suture
10812444027119Suture
10812444027102Suture
10812444026464SUTURE
10812444026105SUTURE
10812444025832SUTURE
10812444024767SUTURE
10812444024750SUTURE
10812444024620SUTURE
10812444024583Suture
10812444024552SUTURE
10812444024422SUTURE
10812444024316SUTURE
10812444024309SUTURE
10812444024293SUTURE
10812444024163SUTURE
10812444024156SUTURE
10812444024149SUTURE
00812444023138SUTURE
10812444023128SUTURE
10812444023111SUTURE
10812444022329SUTURE
10812444020875SUTURE
00812444020861SUTURE
00812444020854SUTURE
00812444020847SUTURE
10812444020837SUTURE
10812444020820SUTURE
10812444020813SUTURE
10812444020806SUTURE
10812444020790SUTURE
10812444020783SUTURE
10812444020776SUTURE
10812444020769SUTURE
10810020082170Suture
10810020084044Suture
10810020084037suture
10810020084020suture
10810020084013suture
10810020082453Suture
10810020082446Suture
10810020082422Suture
10810020084686Suture
10810020084679Suture
10810020081005Suture
10810020080848Suture

Trademark Results [Riverlon]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RIVERLON
RIVERLON
73269349 1199615 Dead/Cancelled
Dan River Inc.
1980-07-07

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