SUPERTORQUE SR3810

GUDID 20705032045893

5F ST .035 65CM MPA

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: 20705032045893
• NIH Device Record Key: 9e716c21-9718-41a8-860d-778f23798151
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUPERTORQUE
• Version Model Number: SR3810
• Catalog Number: SR3810
• 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	10705032045896 [Primary]
GS1	20705032045893 [Package]; Contains: 10705032045896; 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

On-Brand Devices [SUPERTORQUE]

• 20705032026632: CP ST+ 5.2 JL4.5, JR4, PIG
• 20705032020005: 6F .070 JCL 3.5 SH
• 20705032019993: 6F .070 JCL 3.5 100CM
• 20705032019986: 6F .070 JL4.5 ST 100CM
• 20705032019979: 6F .070 JL4 ST 100CM
• 20705032019962: 6F .070 JL3.5 ST 100CM
• 20705032013625: CATH MPAC STP 6F
• 20705032013571: CATH MPAC STP 6F
• 20705032013533: CATH F6 ST+ JR 4 SB 100CM
• 20705032013519: CATH F6 ST+ JR 4 CLASSIC 100CM
• 20705032013502: CATH F6 ST+ CAS III 100CM
• 20705032013489: CATH F6 ST+ CAS II 100CM
• 20705032013472: CATH F6 ST+ CAS I 100CM
• 10705032013628: CATH MPAC STP 6F
• 10705032013574: CATH MPAC STP 6F
• 10705032013536: CATH F6 ST+ JR 4 SB 100CM
• 10705032013512: CATH F6 ST+ JR 4 CLASSIC 100CM
• 10705032013505: CATH F6 ST+ CAS III 100CM
• 10705032011853: CATH ST 5F RIM 65CM
• 10705032011846: CATH ST 5F RC 2 65CM
• 10705032011822: CATH ST 5F HN 4 100CM
• 10705032011815: CATH ST 5F SHK 1.0 65CM
• 10705032011792: CATH ST 5F C3 65CM 2SH
• 10705032011785: CATH ST 5F C2 65CM 2SH
• 10705032011778: CATH ST 5F C1 65CM 2SH
• 10705032011761: CATH ST 5F C3 65CM
• 10705032011754: CATH ST 5F C2 65CM
• 10705032011716: CATH ST 5F RDC A1 80CM
• 10705032011709: CATH ST 5F MP A2 (I) 125CM 2SH
• 10705032011693: CATH ST 5F MP A2 (I) 100CM 2SH
• 10705032011655: CATH ST 5F SIM 2 100CM
• 10705032011648: CATH ST 5F SIM 1 100CM
• 10705032011617: CATH 4F ST MP A2 (I) 100CM 2SH
• 10705032011600: CATH 4F ST RDC A2 (I) 80CM 2SH
• 10705032011594: CATH 4F ST SHK 1.0 65CM
• 10705032011556: CATH 4F ST H1-100CM
• 10705032011549: CATH 4F ST MP A2 (I) 125CM 2SH
• 10705032011532: CATH 4F ST RIM 65CM
• 10705032011525: CATH 4F ST RC 2 65CM
• 10705032011518: CATH 4F ST RC 1 65CM
• 10705032011501: CATH 4F ST C3 65CM 2SH
• 10705032011488: CATH 4F ST C2 65CM 2SH
• 10705032011426: CATH 4F ST J B2 100CM
• 10705032011419: CATH 4F ST J B1 100CM
• 10705032012430: CATH F6 ST CAS III 100CM
• 10705032012416: CATH F6 ST CAS II 100CM
• 10705032012409: CATH F6 ST CAS I 100CM
• 10705032012393: CATH F6 ST CAS III 80CM
• 10705032012386: CATH F6 ST CAS II 80CM
• 10705032012379: CATH F6 ST CAS I 80CM