FDA UDI In Commercial Distribution 🇺🇸 United States

Mega 2000

DI: 10614559100943 · Model: 0825 · MEGADYNE MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Mega 2000
Primary DI
10614559100943
Version / Model
0825
Catalog Number
0825
Company Name
MEGADYNE MEDICAL PRODUCTS, INC.
Labeler DUNS
185444825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-05
Public Version
7
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
ec56ba3b-1322-4612-be98-18d5ae227aa9

Device Description

Reusable Patient Return Electrode, Mega 2000 Sheath, 30 per box

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
11490 Electrosurgical system generator

Identifiers

Type ID
Primary 10614559100943
Package 30614559100947
Package 50614559100941

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K982826 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity