FDA UDI In Commercial Distribution 🇺🇸 United States

ZINGER® MEDIUM

DI: 00763000569556 · Model: ZNGRMS300HS · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ZINGER® MEDIUM
Primary DI
00763000569556
Version / Model
ZNGRMS300HS
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-06
Public Version
1
Public Version Date
2022-02-14
Public Version Status
New
Public Device Record Key
7fec06b6-b000-48ba-b9ed-776a8f97a897

Device Description

GDWR ZNGRMS300HS ZINGERMS 5PK 300 ST 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 20763000569550
Primary 00763000569556

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140695 000

Device Sizes

Type Value Unit Text
Outer Diameter 0.014 Inch
Length 300.0 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dark, dry place.
Type
Special Storage Condition, Specify
Special Conditions
Do not expose to organic solvents.