FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mega Soft

DI: 10614559103142 · Model: M2K-08 · MEGADYNE MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mega Soft
Primary DI
10614559103142
Version / Model
M2K-08
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
2018-09-05
Public Version
7
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
ae5a5303-e340-42a8-8ba3-5878a4aad363
Distribution End Date
2021-12-31

Device Description

Mega Soft Compatibility Cable 2.4 m (8'-0")

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
No
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 10614559103142

Customer Contacts

Phone
+18015769669

Storage Conditions

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