FDA UDI In Commercial Distribution 🇺🇸 United States

WEBSTER

DI: 10846835007367 · Model: F5QL010ST · Biosense Webster Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEBSTER
Primary DI
10846835007367
Version / Model
F5QL010ST
Catalog Number
F5QL010ST
Company Name
Biosense Webster Inc
Labeler DUNS
020163218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
5
Public Version Date
2022-06-07
Public Version Status
Update
Public Device Record Key
840ba5ab-b018-4f2b-b64d-479fe58a6b33

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
DRF CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

GMDN Terms

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

Identifiers

Type ID
Primary 10846835007367

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