FINECROSS NC*A853B

GUDID 54987892058870

FineCross M3 Coronary Micro-Guide Catheter

TERUMO CORPORATION

Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use

• Primary Device ID: 54987892058870
• NIH Device Record Key: 7c879202-5151-4ed1-bad9-ba455cae87d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FINECROSS
• Version Model Number: M3-1430
• Catalog Number: NC*A853B
• Company DUNS: 690543319
• Company Name: TERUMO CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Customer Support Contacts

• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com

Device Dimensions

• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0
• Length: 130 Centimeter
• Outer Diameter: 0.61 Millimeter
• Outer Diameter: 0.84 Millimeter
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987892058875 [Primary]
GS1	54987892058870 [Package]; Contains: 04987892058875; Package: Carton [5 Units]; In Commercial Distribution

FDA Product Code

• DQY: Catheter, percutaneous

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: 2022-06-28
• Device Publish Date: 2022-06-20

On-Brand Devices [FINECROSS]

• 54987350703182: FINECROSS MG Coronary Micro-Guide Catheter
• 54987350703168: FINECROSS MG Coronary Micro-Guide Catheter
• 54987892058870: FineCross M3 Coronary Micro-Guide Catheter
• 54987892058856: FineCross M3 Coronary Micro-Guide Catheter