Baylis Med Tech Passport Steerable Sheath

Basic Information

• Brand Name: Baylis Med Tech Passport Steerable Sheath
• Primary DI: 00885672012533
• Version / Model: PSS0655507D2
• Catalog Number: PSS0655507D2
• Company Name: Oscor Inc.
• Labeler DUNS: 101835833
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-03-15
• Public Version: 1
• Public Version Date: 2023-03-23
• Public Version Status: New
• Public Device Record Key: 93b65e1c-be2f-4aa4-bd89-755f20001ce1

Device Description

Passport Steerable Sheath 6.5F Dual Dilator

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: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• 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
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	00885672012533	GS1

Customer Contacts

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

Premarket Submissions

Submission Number	Supplement Number
K140406	000

Device Sizes

Type	Value	Unit	Text
Device Size Text, specify			Sheath Usable Length 55 cm
Device Size Text, specify			Sheath Overall Length 70 cm
Device Size Text, specify			Curve Length 7 mm
Lumen/Inner Diameter	2.2	Millimeter
Outer Diameter	3.1	Millimeter
Device Size Text, specify			Dilator 1 Overall Length 75 cm Dilator 2 Overall Length 82 cm
Device Size Text, specify			Dilator 1 Usable Length 73 cm Dilator 2 Usable Length 80 cm