FDA UDI In Commercial Distribution 🇺🇸 United States

Navigator

DI: 10815149025312 · Model: 60-3002 · CORPAK MEDSYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Navigator
Primary DI
10815149025312
Version / Model
60-3002
Catalog Number
60-3002
Company Name
CORPAK MEDSYSTEMS, INC.
Labeler DUNS
147530323
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-04
Public Version
3
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
fcc13a0e-fc5a-4cde-b4c3-157e9d63716b

Device Description

Extension cable for use with Navigator

Device Characteristics

Single Use
No
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
44119 Intravascular catheter stylet magnet detector

Identifiers

Type ID
Primary 10815149025312

Customer Contacts