GLIDESHEATH SLENDER TIBIAL PEDAL KIT

Basic Information

• Brand Name: GLIDESHEATH SLENDER TIBIAL PEDAL KIT
• Primary DI: 00389701011912
• Version / Model: 51-1050
• Catalog Number: 51-1050
• Company Name: TERUMO MEDICAL CORPORATION
• Labeler DUNS: 131489882
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2018-08-31
• Public Version: 3
• Public Version Date: 2019-06-07
• Public Version Status: Update
• Public Device Record Key: a1333b91-728b-4828-b751-2b0057a70fbb

Device Description

GLIDESHEATH SLENDER Tibial Pedal Kit

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: Yes
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
DYB	INTRODUCER, CATHETER	Cardiovascular	870.1340	2

GMDN Terms

Code	Name	Definition	Implantable	Status
58865	Vascular catheter introduction set, nonimplantable	A collection of sterile, nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	50389701011917	GS1	Carton	10	In Commercial Distribution
Primary	00389701011912	GS1
Package	30389701011913	GS1	Shelfbox	5	In Commercial Distribution

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Device Sizes

Type	Value	Unit	Text
Device Size Text, specify			Needle: 21/19 Gauge Tapered (0.8/1.1mm) x 2.756" (70 mm)
Device Size Text, specify			Guidewire: 0.021 Inch x 43 Centimeter Nitinol
Length	10	Centimeter
Catheter Gauge	5	French

Storage Conditions

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