FDA UDI In Commercial Distribution 🇺🇸 United States

Zurich Pressure Guidewire System

DI: 00850022994005 · Model: Model 100 · ZURICH MEDICAL INC.
Product Codes
4
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zurich Pressure Guidewire System
Primary DI
00850022994005
Version / Model
Model 100
Catalog Number
308
Company Name
ZURICH MEDICAL INC.
Labeler DUNS
080001248
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-21
Public Version
1
Public Version Date
2020-09-29
Public Version Status
New
Public Device Record Key
b9a51682-4c3b-4613-84d8-41451ffa0c3e

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
DXO Transducer, Pressure, Catheter Tip
DQK Computer, Diagnostic, Programmable
DSK Computer, Blood-Pressure
DQX Wire, Guide, Catheter

GMDN Terms

Code Name
35094 Cardiac/peripheral vascular guidewire, single-use
47486 Intravascular haemodynamic monitoring system guidewire

Identifiers

Type ID
Primary 00850022994005

Premarket Submissions

Submission Number Supplement Number
K190852 000