FDA UDI Not in Commercial Distribution 🇺🇸 United States

MEGADYNE

DI: 10614559104682 · Model: 1900 · MEGADYNE MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEGADYNE
Primary DI
10614559104682
Version / Model
1900
Company Name
MEGADYNE MEDICAL PRODUCTS, INC.
Labeler DUNS
185444825
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-01
Public Version
6
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
da6ccdd2-12c9-4910-9914-7c0e2f58fd54
Distribution End Date
2021-12-31

Device Description

Mega Power Software Calibration Kit

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
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 10614559104682

Customer Contacts

Phone
+18015769669

Premarket Submissions

Submission Number Supplement Number
K050579 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-34 – 65 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity