SUPERTORQUE PLUS SRD7092

GUDID 20705032064924

6F ST+ .038 50CM 12SH PIG

CORDIS CORPORATION

Angiographic catheter, single-use
Primary Device ID20705032064924
NIH Device Record Keyaf6da7da-8673-421c-8e1a-8d26736ea896
Commercial Distribution StatusIn Commercial Distribution
Brand NameSUPERTORQUE PLUS
Version Model NumberSRD7092
Catalog NumberSRD7092
Company DUNS806136177
Company NameCORDIS CORPORATION
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110705032064927 [Primary]
GS120705032064924 [Package]
Contains: 10705032064927
Package: Box [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQOCatheter, intravascular, diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-22
Device Publish Date2024-03-14

On-Brand Devices [SUPERTORQUE PLUS]

207050320766515.2 F ST+ 0.038" 100 CM JL2.5
207050320645115.2F ST+ .038 110CM RBL-4C
207050320632485.2F ST+ 0.038 100CM IM MOD B
20705032062944CATHETER F5.2ST+ 100 CM
207050320628764 F ST+ 0.035" 80CM 4SH PIG
207050320627085.2F ST+ .038 125CM 4SH SON2
20705032012826CATH F5.2ST+ MP A1 100CM
20705032012710CATH F5.2ST+ MPA2(I) 125CM 2SH
20705032012611CATH F5.2+ AL I 100CM
20705032012543CATH F5.2+ MP A2 80CM 2SH
207050320649246F ST+ .038 50CM 12SH PIG
20705032063064CATHETER F6ST+ 100CM
207050320455346F ST+ .038 125CM JL6
20705032026342MULTIPAC ST+ 6 JL4,ARI,PIG145,CSI,GW
20705032026335MULTIPAC ST+ 6 JL4,ARI,PIG,CSI,GW

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