FDA UDI In Commercial Distribution 🇺🇸 United States

OCTARAY Mapping Catheter

DI: 10846835021141 · Model: D160901 · Biosense Webster Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OCTARAY Mapping Catheter
Primary DI
10846835021141
Version / Model
D160901
Catalog Number
D160901
Company Name
Biosense Webster Inc
Labeler DUNS
020163218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-14
Public Version
2
Public Version Date
2022-02-10
Public Version Status
Update
Public Device Record Key
d87e24f1-1b2b-4a86-8234-9858847530b8

Device Description

OCTA,PERSEID,2-2-2-2-2,D-CURVE

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MTD Catheter, intracardiac mapping, high-density array

GMDN Terms

Code Name
46355 Cardiac mapping catheter, percutaneous, single-use

Identifiers

Type ID
Primary 10846835021141

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K193237 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep out of direct sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged
Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is opened