SUPERTORQUE PLUS 533557

GUDID 20705032012710

CATH F5.2ST+ MPA2(I) 125CM 2SH

CORDIS CORPORATION

Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use

• Primary Device ID: 20705032012710
• NIH Device Record Key: e72caff1-5e4c-4b86-b1ba-802ad5db0eae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUPERTORQUE PLUS
• Version Model Number: 533557
• Catalog Number: 533557
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705032012713 [Primary]
GS1	20705032012710 [Package]; Contains: 10705032012713; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• DQO: Catheter, intravascular, diagnostic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-04
• Device Publish Date: 2024-02-23

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• 20705032062944: CATHETER F5.2ST+ 100 CM
• 20705032062876: 4 F ST+ 0.035" 80CM 4SH PIG
• 20705032062708: 5.2F ST+ .038 125CM 4SH SON2
• 20705032012826: CATH F5.2ST+ MP A1 100CM
• 20705032012710: CATH F5.2ST+ MPA2(I) 125CM 2SH
• 20705032012611: CATH F5.2+ AL I 100CM
• 20705032012543: CATH F5.2+ MP A2 80CM 2SH
• 20705032064924: 6F ST+ .038 50CM 12SH PIG
• 20705032063064: CATHETER F6ST+ 100CM
• 20705032045534: 6F ST+ .038 125CM JL6
• 20705032026342: MULTIPAC ST+ 6 JL4,ARI,PIG145,CSI,GW
• 20705032026335: MULTIPAC ST+ 6 JL4,ARI,PIG,CSI,GW