FDA UDI In Commercial Distribution 🇺🇸 United States

J-PLASMA® PRECISE™

DI: 00607151010720 · Model: BVX-330BR · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
J-PLASMA® PRECISE™
Primary DI
00607151010720
Version / Model
BVX-330BR
Catalog Number
BVX-330BR
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
4
Public Version Date
2019-02-21
Public Version Status
Update
Public Device Record Key
81f1ad65-8384-492e-9fe6-f948928e3d51

Device Description

J-PLASMA® PRECISE™ 360 LAPAROSCOPIC HAND DEVICE WITH BLADE, 33cm

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
Yes
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
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Package 10607151010727
Primary 00607151010720

Premarket Submissions

Submission Number Supplement Number
K152570 000