FDA UDI In Commercial Distribution 🇺🇸 United States

Quick-Cross Extreme

DI: 00813132021474 · Model: 518-078AB · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Quick-Cross Extreme
Primary DI
00813132021474
Version / Model
518-078AB
Catalog Number
518-078
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-04-06
Public Version
8
Public Version Date
2023-08-04
Public Version Status
Update
Public Device Record Key
5a6b2cea-f571-4c0c-9cc6-50652d1c6bc9

Device Description

Quick-Cross Extreme Support 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
No

Product Codes

Code Name
DQY Catheter, Percutaneous

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Secondary M204518078AB0
Primary 00813132021474
Package 20813132021478

Customer Contacts

Device Sizes

Type Value Unit Text
Length 90 Centimeter
Lumen/Inner Diameter 0.035 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry