FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 06948806311033 · Model: F6010252065PRT · Synaptic Medical, Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
06948806311033
Version / Model
F6010252065PRT
Company Name
Synaptic Medical, Ltd.
Labeler DUNS
421256891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-17
Public Version
1
Public Version Date
2018-06-18
Public Version Status
New
Public Device Record Key
309980b2-99bc-413f-941f-9913ea12e9b8

Device Description

Electrophysiology Catheter

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
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 06948806311033