CEREGLIDE SBC92114UG

GUDID 10886704086017

CEREGLIDE 92 Catheter System CEREGLIDE 92 INNERGLIDE 9 114 cm 165 cm 0.092 in (2.34 mm) 0.030 in (0.76 mm) 0.102 in (2.59 mm) 0.042 in (1.07 mm) 0.108 in (2.74 mm) 0.078 in (1.98 mm) 0.113 in (2.87 mm) Minimum Guide Diameter

Cerenovus, Inc.

Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use

• Primary Device ID: 10886704086017
• NIH Device Record Key: 6bf61c94-4f20-427f-8b2f-9dc8770de9e5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CEREGLIDE
• Version Model Number: SBC92114UG
• Catalog Number: SBC92114UG
• Company DUNS: 607846297
• Company Name: Cerenovus, Inc.
• 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704086017 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230726

FDA Product Code

• QJP: Catheter, Percutaneous, Neurovasculature

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: 2024-06-28
• Device Publish Date: 2024-06-20

On-Brand Devices [CEREGLIDE]

• 10886704086109: CEREGLIDE 92 Catheter System CEREGLIDE 92 INNERGLIDE 9 135 cm 165 cm 0.092 in (2.34 mm) 0.030 i
• 10886704086079: CEREGLIDE 92 Catheter System CEREGLIDE 92 INNERGLIDE 9 130 cm 165 cm 0.092 in (2.34 mm) 0.030
• 10886704086048: CEREGLIDE 92 Catheter System CEREGLIDE 92 INNERGLIDE 9 122 cm 165 cm 0.092 in (2.34 mm) 0.030
• 10886704086017: CEREGLIDE 92 Catheter System CEREGLIDE 92 INNERGLIDE 9 114 cm 165 cm 0.092 in (2.34 mm) 0.030