FDA UDI In Commercial Distribution 🇺🇸 United States

GuideRight™

DI: 05414734013673 · Model: 405050 · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GuideRight™
Primary DI
05414734013673
Version / Model
405050
Catalog Number
405050
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-30
Public Version
4
Public Version Date
2020-09-21
Public Version Status
Update
Public Device Record Key
82adeea4-f26a-4c83-84a8-e6e0a57631f4

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
DQX WIRE, GUIDE, CATHETER

GMDN Terms

Code Name
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Package 15414734013670
Primary 05414734013673

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.89 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
STORE IN A COOL, DARK, DRY PLACE.