FDA UDI In Commercial Distribution 🇺🇸 United States

Mega Soft

DI: 10614559105252 · Model: M2K09 · MEGADYNE MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mega Soft
Primary DI
10614559105252
Version / Model
M2K09
Catalog Number
M2K09
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
10
Public Version Date
2023-05-12
Public Version Status
Update
Public Device Record Key
429e7d94-9a0c-4608-a54b-168db070285b

Device Description

Mega Soft Compatibility Cable 4.4 m (14'-5")

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
63401 Electrosurgical return lead

Identifiers

Type ID
Primary 10614559105252
Package 30614559105256

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080741 000
K133726 000

Storage Conditions

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