CARDIOXYL ®

GUDID 13661522016265

PETERS SURGICAL

Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament
Primary Device ID13661522016265
NIH Device Record Keya5505fb4-058e-4096-9ea4-b828edfbe67e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCARDIOXYL ®
Version Model Number73P30Y
Company DUNS265741780
Company NamePETERS SURGICAL
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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
GS103661522016268 [Primary]
GS113661522016265 [Package]
Contains: 03661522016268
Package: [12 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

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 Date2020-01-17
Device Publish Date2020-01-09

On-Brand Devices [CARDIOXYL ®]

1366152201449073S20G
1366152201444573S15G
1366152201443873S10C
1366152201430873P35A
1366152201429273S15F
1366152201413173S20F
1366152201411773P30V
1366152201410073P30U
1366152201217573S30Y
1366152201216873S30X
1366152201215173S30W
1366152201214473S30V
1366152201213773S30U
1366152201212073S30T
1366152201211373S30R
1366152201210673S30Q
1366152201209073S30P
1366152201208373S30O
1366152201207673S30N
1366152201206973S30M
1366152201205273S30C
1366152201204573S30B
1366152201203873S30AB
1366152201202173S30AA
1366152201201473S30A
1366152201200773S20E
1366152201199473S20D
1366152201198773S20B
1366152201197073S20A
1366152201196373S15C
1366152201195673P30T
1366152201194973P30S
1366152201193273P30R
1366152201192573P30Q
1366152201191873P30P
1366152201190173P30O
1366152201189573P30L
1366152201188873P30K
1366152201187173P30J
1366152201186473P30I
1366152201185773P30G
1366152201184073P30F
1366152201183373P30E
1366152201182673P30D
1366152201181973P30B
1366152201180273P30A
1366152201178973S15B
1366152210005673P30DS
1366152204449773P30DR
1366152204314873P30DW
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