FDA UDI In Commercial Distribution 🇺🇸 United States

SUPER TORQUE

DI: 10705032046275 · Model: SR4483 · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SUPER TORQUE
Primary DI
10705032046275
Version / Model
SR4483
Catalog Number
SR4483
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
6
Public Version Date
2022-09-14
Public Version Status
Update
Public Device Record Key
5854c4d9-052f-4006-98ca-be4e3326002e

Device Description

5.2 F ST+ 0.038 INCHES 80CM VENOGRA

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
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Primary 10705032046275
Package 20705032046272

Premarket Submissions

Submission Number Supplement Number
K914007 000