VISIGLIDE N3622831

GUDID 54953170465081

VISIGLIDE Single Use Guidewire

TERUMO CORPORATION

Gastro-urological guidewire, single-use

• Primary Device ID: 54953170465081
• NIH Device Record Key: e2f0cc4d-a54e-44f5-bb46-37c6cbd2e161
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VISIGLIDE
• Version Model Number: G-240-3545A
• Catalog Number: N3622831
• Company DUNS: 690543319
• Company Name: TERUMO CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Customer Support Contacts

• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx

Device Dimensions

• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4500 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 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170465086 [Primary]
GS1	54953170465081 [Package]; Contains: 04953170465086; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• OCY: Endoscopic guidewire, gastroenterology-urology

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: 2025-07-22
• Device Publish Date: 2025-07-14

On-Brand Devices [VISIGLIDE]

• 54953170282886: VISIGLIDE Single Use Guidewire
• 54953170282862: VISIGLIDE Single Use Guidewire
• 54953170282848: VISIGLIDE Single Use Guidewire
• 54953170282824: VISIGLIDE Single Use Guidewire
• 54953170282800: VISIGLIDE Single Use Guidewire
• 54953170282787: VISIGLIDE Single Use Guidewire
• 54953170282763: VISIGLIDE Single Use Guidewire
• 54953170282749: VISIGLIDE Single Use Guidewire
• 54953170465128: VISIGLIDE Single Use Guidewire
• 54953170465111: VISIGLIDE Single Use Guidewire
• 54953170465104: VISIGLIDE Single Use Guidewire
• 54953170465098: VISIGLIDE Single Use Guidewire
• 54953170465081: VISIGLIDE Single Use Guidewire
• 54953170465074: VISIGLIDE Single Use Guidewire
• 54953170465067: VISIGLIDE Single Use Guidewire
• 54953170465050: VISIGLIDE Single Use Guidewire