FDA UDI In Commercial Distribution 🇺🇸 United States

StarBurst

DI: H7877001039081 · Model: 700-103908 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
StarBurst
Primary DI
H7877001039081
Version / Model
700-103908
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
6e7ffeae-73e9-49f1-91c2-3e1ee02902ee

Device Description

RITA StarBurst SDE Electrosurgical Device

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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
61933 Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

Identifiers

Type ID
Primary H7877001039081
Secondary 15051684021814

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K030967 000

Device Sizes

Type Value Unit Text
Length 12 Centimeter