CEREGLIDE

Basic Information

• Brand Name: CEREGLIDE
• Primary DI: 10886704088141
• Version / Model: CS71132U
• Catalog Number: CS71132U
• Company Name: Cerenovus, Inc.
• Labeler DUNS: 607846297
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2025-10-13
• Public Version: 1
• Public Version Date: 2025-10-21
• Public Version Status: New
• Public Device Record Key: ad250f46-deb7-4f9c-b6b9-2db5f8a35637

Device Description

CEREGLIDE 71 INNERGLIDE 7 132 cm 165 cm 0.071 in (1.80 mm) 0.030 in (0.76 mm) 0.082 in (2.08 mm) 0.042 in (1.07 mm) 0.0825 in (2.10 mm) 0.059 in (1.50 mm) 0.085 in (2.16 mm) Minimum Guide Diameter

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
QJP	Catheter, Percutaneous, Neurovasculature	Cardiovascular	870.1250	2
NRY	CATHETER, THROMBUS RETRIEVER	Cardiovascular	870.1250	2

GMDN Terms

Code	Name	Definition	Implantable	Status
17846	Vascular guide-catheter, single-use	A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	10886704088141	GS1

Customer Contacts

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

Premarket Submissions

Submission Number	Supplement Number
K251828	000