FDA UDI In Commercial Distribution 🇺🇸 United States

SUPER TORQUE

DI: 20705032046630 · Model: SR4862 · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SUPER TORQUE
Primary DI
20705032046630
Version / Model
SR4862
Catalog Number
SR4862
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
2022-08-10
Public Version Status
Update
Public Device Record Key
72ab48c8-2f54-4854-9295-f3d1317e02dc

Device Description

4F ST .035 65CM 6SH GENSINI

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 20705032046630

Premarket Submissions

Submission Number Supplement Number
K914007 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damanged
Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dark, dry place