FDA UDI In Commercial Distribution 🇺🇸 United States

LATITUDE® Clarity

DI: 00802526613838 · Model: 7260 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LATITUDE® Clarity
Primary DI
00802526613838
Version / Model
7260
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
106295384
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-01
Public Version
2
Public Version Date
2023-09-27
Public Version Status
Update
Public Device Record Key
5bdfca1c-110d-4b03-9be2-70fb43fa4a5f

Device Description

Device Services Software

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MXD Recorder, event, implantable cardiac, (with arrhythmia detection)

GMDN Terms

Code Name
44106 Patient health record information system application software

Identifiers

Type ID
Primary 00802526613838