FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 06948806311019 · Model: F6004005115ART · Synaptic Medical, Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
06948806311019
Version / Model
F6004005115ART
Catalog Number
F6004005115ART
Company Name
Synaptic Medical, Ltd.
Labeler DUNS
421256891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b7de1ced-5e83-40e4-9bec-f6aab3c0f67a

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
Yes
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 06948806311019

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 6 French