FDA UDI In Commercial Distribution 🇺🇸 United States

OPTEASE

DI: 20705032009369 · Model: 466C210F · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OPTEASE
Primary DI
20705032009369
Version / Model
466C210F
Catalog Number
466C210F
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-18
Public Version
9
Public Version Date
2022-08-12
Public Version Status
Update
Public Device Record Key
237769d1-fd01-4d42-96db-b96b3aa4923d

Device Description

10FR OPTEASE RETRIEVAL CATH.

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
Yes
MRI Safety
MR Conditional
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
DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR

GMDN Terms

Code Name
17927 Intravascular extraction catheter-snare

Identifiers

Type ID
Primary 20705032009369

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius