FDA UDI In Commercial Distribution 🇺🇸 United States

CORDIS

DI: 20705032047491 · Model: SRA0203 · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CORDIS
Primary DI
20705032047491
Version / Model
SRA0203
Catalog Number
SRA0203
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
8
Public Version Date
2022-08-10
Public Version Status
Update
Public Device Record Key
ed5b5302-18ac-4f22-a1a3-7929105ec828

Device Description

CSIS 8F BTS 65CM JCURVE 3D

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DYB INTRODUCER, CATHETER

GMDN Terms

Code Name
36079 Haemostasis valve

Identifiers

Type ID
Primary 20705032047491

Storage Conditions

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