INFINITI CP0418

GUDID 10705032026673

MULTIPAC INF 4F JL5, ARMOD,

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: 10705032026673
• NIH Device Record Key: 78134627-5519-4e1a-b6ef-27bc540b782f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INFINITI
• Version Model Number: CP0418
• Catalog Number: CP0418
• 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	10705032026673 [Primary]
GS1	20705032026670 [Package]; Package: BOX [10 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 [INFINITI]

• 20705032073896: 4F INF 0.038 INCHES 100CM 2SH RBL4
• 20705032073889: INFINITI F4 110 CM 0.038"GW
• 20705032073872: IF 4F .038 100CM IM MODIFIED
• 20705032073865: 5F INF .038 100CM AL .75
• 20705032073858: IF 4F .038 110CM 9 SH PIG
• 20705032073841: TI 6F.038 110CM LEFT COR 4.5CM
• 20705032073834: TI 6F.038 110CM LEFT COR 5CM
• 20705032073827: TI 6F .038 110CM RT CORONARY
• 20705032073810: TI 6F .038 100CM CHAMP 3
• 20705032073803: 6F INF 0.038 INCHES 100CM RBL 4
• 20705032073797: 5F INF 0.038 INCHES 100CM RBL5
• 20705032073780: 6F INF .038 50 CM
• 20705032073773: 6F INF 0.038 INCHES 100CM RBL5
• 20705032073766: 4F INF .038
• 20705032073759: 6F INF .038 100 CM
• 20705032073742: TI 6F.038 110CM LEFT COR 3.5CM
• 20705032073735: 4F INF 0.038 INCHES 100CM 2SH RBL5
• 20705032073711: IF INF F4 .038 INCHES 100CM RBMP
• 20705032073704: 6 F INF 0.038 INCHES 100CM JR4 MOD.
• 20705032073698: CATHETER F4 INF 100 CM
• 20705032073681: 4 INF 110 SON2
• 20705032073674: INFINITI F5 100CM .038GW
• 20705032073667: 5F INF 0.038 100CM SIM3
• 20705032073643: TL 5F .038 80CM MPA
• 20705032073636: 5F INF 0.038 INCHES 100CM RBL4
• 20705032073032: MULTIPAC 5F JL3.5, JR4
• 20705032073001: 6F INF 0.038 INCHES 100CM 2SH RBL5
• 20705032072981: 5F INF 0.038 100CM SIM2
• 20705032072943: 5F INF .038 INCHES 110CM RBL4
• 20705032072936: 5F INF 0.038 INCHES 100CM 2SH RBL4
• 20705032072929: 6F INF 0.038 INCHES 100CM 2SH RBL4
• 20705032072905: 5F INF 0.038 INCHES 100CM 2SH RBL5
• 20705032072714: 5F INF .038 100CM AR3
• 20705032072677: 6F INF .038 115CM 1SH LEMAN
• 20705032072660: 6F INF .038 115CM 1SH RBMP
• 20705032072653: 6F INF .038 115CM 1SH RBL-A
• 20705032072615: CP 4F INF JR4 XB3.5
• 20705032072608: 4F INF .038 100CM IMMOD
• 20705032071793: 6F INF .038 100CM RBL3.5
• 20705032068045: 5F INF .038 100CM 2SH JR4
• 20705032068038: 4F INF .038 65CM JR2.5
• 20705032068021: 4F INF .038 65CM JR2
• 20705032068014: 4F INF .038 65CM JL2.5
• 20705032068007: 4F INF .038 65CM JL2
• 20705032067932: 5F INF .038 65CM Z-AL2
• 20705032067840: 6F INF .038 100CM JCL4
• 20705032067833: 6F INF .038 100CM JCL3.5
• 20705032064979: 5F INF .038 100CM JCL4
• 20705032064962: 5F INF .038 100CM JCL3.5
• 20705032064955: 4F INF .038 100CM JCL4