FDA UDI Not in Commercial Distribution 🇺🇸 United States

THUNDER®

DI: 00643169452343 · Model: LVTNDR190S · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
THUNDER®
Primary DI
00643169452343
Version / Model
LVTNDR190S
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-04
Public Version
4
Public Version Date
2023-03-16
Public Version Status
Update
Public Device Record Key
47022490-22b1-4b62-a293-5ae534502daa
Distribution End Date
2022-12-13

Device Description

GDWR LVTNDR190S THNDR CRM 5PK 190 ST SIL

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
No
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 20643169452347
Primary 00643169452343

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140695 000

Device Sizes

Type Value Unit Text
Length 190.0 Centimeter
Outer Diameter 0.014 Inch