FDA UDI Not in Commercial Distribution 🇺🇸 United States

Turbo Elite™

DI: M204425135010 · Model: 425-135-01 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Turbo Elite™
Primary DI
M204425135010
Version / Model
425-135-01
Catalog Number
425-135-01
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-08-28
Public Version
4
Public Version Date
2021-10-26
Public Version Status
Update
Public Device Record Key
a5bad744-7b42-4b8e-a780-aa39b437b401
Distribution End Date
2019-02-06

Device Description

Turbo-Elite™ Laser Atherectomy 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
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MCW Catheter, Peripheral, Atherectomy

GMDN Terms

Code Name
43229 Atherectomy laser system beam guide-catheter, peripheral

Identifiers

Type ID
Primary M204425135010

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 2.6 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 140 Degrees Fahrenheit