DUALVIEW TU*DV01U

GUDID 04987350744487

Imaging Catheter

TERUMO CORPORATION

Intravascular ultrasound imaging catheter, single-use

• Primary Device ID: 04987350744487
• NIH Device Record Key: e71d4218-68b8-4b7d-a6f8-943c21d87312
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUALVIEW
• Version Model Number: TU-DSS01C
• Catalog Number: TU*DV01U
• 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: true
• 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
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.This way up.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987350744487 [Primary]
GS1	54987350744482 [Package]; Package: Carton [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: 2026-01-29
• Device Publish Date: 2026-01-21

Devices Manufactured by TERUMO CORPORATION

• 04987350740601 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 04987350740625 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 04987350740649 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 54987350740668 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 04987350740687 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 54987350740699 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 04987350740700 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire
• 04987350745422 - GLIDEWIRE GT-R: 2026-02-16 Glidewire GT-R Guide Wire