FDA UDI In Commercial Distribution 🇺🇸 United States

ZINGER® MEDIUM

DI: 00643169452305 · Model: LVZRMS180S · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ZINGER® MEDIUM
Primary DI
00643169452305
Version / Model
LVZRMS180S
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
46657db8-32ab-424e-a4d1-2e2152eb60c8

Device Description

GDWR LVZRMS180S ZINGRMS CRM 5PK 180 S HY

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 20643169452309
Primary 00643169452305

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140695 000

Device Sizes

Type Value Unit Text
Outer Diameter 0.014 Inch
Length 180.0 Centimeter