GLIDESHEATH SLENDER TIBIAL PEDAL KIT 52-1050

GUDID 30389701012347

GLIDESHEATH SLENDER Tibial Pedal Kit, 40mm

TERUMO MEDICAL CORPORATION

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• Primary Device ID: 30389701012347
• NIH Device Record Key: 009a41a2-0427-46b1-a7bb-3b0bda8b2be2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GLIDESHEATH SLENDER TIBIAL PEDAL KIT
• Version Model Number: 52-1050
• Catalog Number: 52-1050
• Company DUNS: 131489882
• Company Name: TERUMO MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: true
• 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

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
• 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: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Gauge: 5 French
• Length: 10 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity
• Special Storage Condition, Specify: Between 0 and 0 *Avoid direct sunlight. Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00389701012346 [Primary]
GS1	30389701012347 [Package]; Contains: 00389701012346; Package: Shelfpack [5 Units]; In Commercial Distribution
GS1	50389701012341 [Package]; Contains: 00389701012346; Package: Carton [10 Units]; In Commercial Distribution

FDA Product Code

• DYB: INTRODUCER, CATHETER

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: 2020-02-21
• Device Publish Date: 2020-02-13

On-Brand Devices [GLIDESHEATH SLENDER TIBIAL PEDAL KIT]

• 50389701011917: GLIDESHEATH SLENDER Tibial Pedal Kit
• 30389701012347: GLIDESHEATH SLENDER Tibial Pedal Kit, 40mm