FDA UDI In Commercial Distribution 🇺🇸 United States

Navilyst

DI: H965970004010 · Model: 97000401 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Navilyst
Primary DI
H965970004010
Version / Model
97000401
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2022-05-16
Public Version Status
Update
Public Device Record Key
5ddf7b71-7867-471b-8e0a-6262d91ba712

Device Description

Angiographic Guidewire, Fixed Core, Straight Tip

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
DQX WIRE, GUIDE, CATHETER

GMDN Terms

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

Identifiers

Type ID
Package H965970004011
Primary H965970004010

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.035 Inch
Length 260 Centimeter