FDA UDI Not in Commercial Distribution 🇺🇸 United States

Turbo-Booster™

DI: M2045180430 · Model: 518-043 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Turbo-Booster™
Primary DI
M2045180430
Version / Model
518-043
Catalog Number
518-043
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-15
Public Version
9
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
4fc92a7d-44ed-4757-85b9-15529b219106
Distribution End Date
2019-02-06

Device Description

Turbo-Booster™ Laser Guide Catheter

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
PDU Catheter For Crossing Total Occlusions

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Package M2045180431
Primary M2045180430

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071226 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 0.094 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 140 Degrees Fahrenheit