FDA UDI In Commercial Distribution 🇺🇸 United States

STORQ

DI: 10705032055901 · Model: 503356Y · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
STORQ
Primary DI
10705032055901
Version / Model
503356Y
Catalog Number
503356Y
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-26
Public Version
2
Public Version Date
2022-02-15
Public Version Status
Update
Public Device Record Key
f26d15da-3e53-45b5-a3d7-bd2ba5f5f823

Device Description

SGW STORQ .035 300CM ANGLED S

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 20705032055908
Primary 10705032055901