FDA UDI In Commercial Distribution 🇺🇸 United States

BOVIE®

DI: 00607151012151 · Model: H10008 · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BOVIE®
Primary DI
00607151012151
Version / Model
H10008
Catalog Number
H10008
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-15
Public Version
3
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
46d9078c-1ffc-4af6-995d-ecb588558213

Device Description

H-TYPE SHARP TIP DISPOSABLE DERMAL ELECTRODE, STERILE

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
HGI Electrocautery, Gynecologic (And Accessories)

GMDN Terms

Code Name
61874 Open-surgery electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Package 10607151012158
Primary 00607151012151