FDA UDI In Commercial Distribution 🇺🇸 United States

WECK

DI: 00607151009809 · Model: 809319 · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
WECK
Primary DI
00607151009809
Version / Model
809319
Catalog Number
809319
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-02
Public Version
3
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
24a4c7cc-eb9a-4629-9527-31c12bde3e43

Device Description

DISPOSABLE 6” EXTENDED ¾” BLADE ELECTRODE 24/BX, 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
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

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

Identifiers

Type ID
Primary 00607151009809
Package 10607151009806