FDA UDI In Commercial Distribution 🇺🇸 United States

Quick-Cross Extreme

DI: 00813132029425 · Model: 518-086-B · Philips Image Guided Therapy Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Quick-Cross Extreme
Primary DI
00813132029425
Version / Model
518-086-B
Catalog Number
518-086
Company Name
Philips Image Guided Therapy Corporation
Labeler DUNS
118354223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-04
Public Version
1
Public Version Date
2023-10-12
Public Version Status
New
Public Device Record Key
02e033bd-1344-4ce7-9530-c47d1a1b1d74

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
Yes
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
Package 20813132029429
Primary 00813132029425

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150201 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 0.014 Inch
Length 150 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight