FH Link

GUDID 00840277405838

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament
Primary Device ID00840277405838
NIH Device Record Key0eafe32b-2017-42a2-9e78-851086eb7853
Commercial Distribution StatusIn Commercial Distribution
Brand NameFH Link
Version Model NumberHS168
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
GS100840277405838 [Primary]

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 Date2024-11-01
Device Publish Date2024-10-24

Devices Manufactured by RIVERPOINT MEDICAL, LLC

10840277405774 - Vilet II2024-11-12 Suture
10840277405781 - Vilet II2024-11-12 Suture
10840277405354 - Vilet II2024-11-11 Suture
10840277405736 - Vilet II2024-11-11 Suture
00840277405746 - Vilet II2024-11-11 Suture
10840277405750 - Vilet II2024-11-11 Suture
10840277405767 - Vilet II2024-11-11 Suture
00840277405968 - ARTHROLINK2024-11-07 Suture

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