FDA UDI In Commercial Distribution 🇺🇸 United States

LIGHTWAVE

DI: 20845854040369 · Model: IA-2379-FC · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LIGHTWAVE
Primary DI
20845854040369
Version / Model
IA-2379-FC
Catalog Number
IA-2379-FC
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2024-08-14
Public Version Status
Update
Public Device Record Key
d99c2e9e-e98a-41ae-ab1e-19349613bec2

Device Description

LIGHTWAVE ABLATOR, 90° ANGLE, 3.2MM X 150 MM

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

Identifiers

Type ID
Primary 20845854040369

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083281 000

Device Sizes

Type Value Unit Text
Width 3.2 Millimeter
Length 150 Millimeter