FDA UDI Not in Commercial Distribution 🇺🇸 United States

WEBSTER

DI: 10846835001549 · Model: 111842RT · Biosense Webster Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEBSTER
Primary DI
10846835001549
Version / Model
111842RT
Catalog Number
111842RT
Company Name
Biosense Webster Inc
Labeler DUNS
020163218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
9
Public Version Date
2023-06-01
Public Version Status
Update
Public Device Record Key
99674f63-1b09-4bec-9206-a59be113b19e
Distribution End Date
2023-06-01

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
LDF ELECTRODE, PACEMAKER, TEMPORARY

GMDN Terms

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

Identifiers

Type ID
Primary 10846835001549

Customer Contacts

Storage Conditions

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
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Special Storage Condition, Specify
Special Conditions
Keep out of direct sunlight