FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 10846835005608 · Model: D7DL252RT · Biosense Webster Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
10846835005608
Version / Model
D7DL252RT
Catalog Number
D7DL252RT
Company Name
Biosense Webster Inc
Labeler DUNS
020163218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-10
Public Version
6
Public Version Date
2022-06-07
Public Version Status
Update
Public Device Record Key
1ced1428-3700-4b58-a119-624c277e58ca

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
LPB Cardiac ablation percutaneous catheter

GMDN Terms

Code Name
61785 Cardiac radio-frequency ablation system catheter

Identifiers

Type ID
Primary 10846835005608

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P950005 000

Storage Conditions

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