SUTUMED

GUDID 07757093059547

Unilene S.A.C.

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 ID07757093059547
NIH Device Record Key57c12382-5356-4939-bf5a-8a3b47799693
Commercial Distribution StatusIn Commercial Distribution
Brand NameSUTUMED
Version Model NumberSDPP020MC360
Company DUNS934900072
Company NameUnilene S.A.C.
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com
Phone+051()997509089
Emailmarthalujan@unilene.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107757093024125 [Primary]
GS107757093059547 [Package]
Contains: 07757093024125
Package: BOX [12 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GAWSuture, Nonabsorbable, Synthetic, Polypropylene

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-06-02
Device Publish Date2023-01-07

On-Brand Devices [SUTUMED]

07757093038375POLYGLACTIN
07757093036913POLYGLACTIN
07757093067214SDST070TE065
07757093684336SDPP001MC250
07757093680642SDPP060TC190
07757093652939SDPP010TC240
07757093652731SDPP001TC190
07757093325772SDPP001MC360
07757093218425SDPP001TC370
07757093061939SDPP070TS093
07757093061700SDPP060TR130
07757093061571SDPP060TC160
07757093061557SDPP060TC130
07757093061465SDPP060MR150
07757093061250SDPP050TR130
07757093061168SDPP050TC190
07757093061144SDPP050TC160
07757093061120SDPP050TC130
07757093061038SDPP050MR170
07757093060888SDPP050MC160
07757093060734SDPP040TC240
07757093060710SDPP040TC190
07757093060604SDPP040MR260
07757093060567SDPP040MR200
07757093060536SDPP040MR170
07757093060512SDPP040MR150
07757093060291SDPP030TC260
07757093060277SDPP030TC240
07757093060246SDPP030TC190
07757093060185SDPP030RC600
07757093060109SDPP030MR260
07757093060093SDPP030MR250
07757093060000SDPP030MC260
07757093059998SDPP030MC250
07757093059851SDPP020TC400
07757093059806SDPP020TC240
07757093059783SDPP020TC190
07757093059752SDPP020RC600
07757093059677SDPP020MR350
07757093059639SDPP020MR260
07757093059547SDPP020MC360
07757093059530SDPP020MC350
07757093059523SDPP020MC260
07757093059455SDPP010TC400
07757093059387SDPP010RC600
07757093059318SDPP010MR400
07757093059288SDPP010MR360
07757093059257SDPP010MR260
07757093059189SDPP010MC360
07757093058922SDPP001MR400

Trademark Results [SUTUMED]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SUTUMED
SUTUMED
87158058 not registered Dead/Abandoned
SUTUMED CORP.
2016-09-01

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