CYTOSURG

GUDID 10810020084624

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament
Primary Device ID10810020084624
NIH Device Record Key7230b71f-479d-49aa-96bd-27e1183b628b
Commercial Distribution StatusIn Commercial Distribution
Brand NameCYTOSURG
Version Model NumberT8664C
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
GS100810020084627 [Primary]
GS110810020084624 [Package]
Contains: 00810020084627
Package: [12 Units]
In Commercial Distribution

FDA Product Code

NBYSuture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-09
Device Publish Date2020-09-01

On-Brand Devices [CYTOSURG]

10812444020097SUTURE
10812444020080SUTURE
10812444020073SUTURE
10812444020066SUTURE
10812444020059SUTURE
10812444020042SUTURE
10812444020035SUTURE
10812444020028SUTURE
10812444020011SUTURE
10810020084662Suture
10810020084655Suture
10810020084648Suture
10810020084631Suture
10810020084624Suture
10810020084617Suture
10810020084600Suture
00810020084597Suture
10810020084587Suture

Trademark Results [CYTOSURG]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CYTOSURG
CYTOSURG
87159559 5297981 Live/Registered
Salvin Dental Specialties, Inc.
2016-09-02

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