DUCOR 527792N

GUDID 10705032011167

CATH MPAC 7FHF JR4,JL4,PIG

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

• Primary Device ID: 10705032011167
• NIH Device Record Key: 0d518523-2c9a-455b-a999-7df361227e1b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUCOR
• Version Model Number: 527792N
• Catalog Number: 527792N
• 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	10705032011167 [Primary]
GS1	20705032011164 [Package]; Package: BOX [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K862006

FDA Product Code

• DQO: CATHETER, INTRAVASCULAR, DIAGNOSTIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-02-15
• Device Publish Date: 2016-08-01

On-Brand Devices [DUCOR]

• 20705032014561: INF TL PROPAC FR6
• 20705032014554: INF TL PROPAC FR6
• 20705032014547: INF TL PROPAC FR6
• 20705032014530: INF TL PROPAC FR6
• 20705032014127: CATH PROPAC 5F INF 035GW
• 20705032014110: CATH PROPAC 5F INF 038GW
• 20705032014103: CATH PROPAC 5FINF 035GW PIG145
• 20705032014097: CATH PROPAC 5FINF 038GW PIG145
• 10705032014564: INF TL PROPAC FR6
• 10705032014557: INF TL PROPAC FR6
• 10705032014120: CATH PROPAC 5F INF 035GW
• 10705032014113: CATH PROPAC 5F INF 038GW
• 10705032014106: CATH PROPAC 5FINF 035GW PIG145
• 10705032014090: CATH PROPAC 5FINF 038GW PIG145
• 10705032014540: INF TL PROPAC FR6
• 10705032014533: INF TL PROPAC FR6
• 10705032012362: CATH MPAC 6F ST JL4,JR4,PIG
• 10705032011167: CATH MPAC 7FHF JR4,JL4,PIG
• 10705032011099: CATH MPAC 7FHF JL4,JR4,PIG