Guide Glide II® Guidewire Introducer Needle

Basic Information

• Brand Name: Guide Glide II® Guidewire Introducer Needle
• Primary DI: M661S010212753
• Version / Model: S01021-2.753L
• Company Name: Spectra Medical Devices, LLC
• Labeler DUNS: 118301171
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2024-02-12
• Public Version: 1
• Public Version Date: 2024-02-20
• Public Version Status: New
• Public Device Record Key: b7d5ebfe-f6f1-4543-a14a-d62b1ad9bd84

Device Description

1ga x 2.75", A-Bevel, Clear Plastic Hub, Lubricated, Wing

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• 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: No
• 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
Primary	M661S010212753	HIBCC

Premarket Submissions

Submission Number	Supplement Number
K082580	000