FDA UDI In Commercial Distribution 🇺🇸 United States

MEGA PLUS SPINE SYSTEM

DI: 08809763501852 · Model: 14100 · BK MEDITECH CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MEGA PLUS SPINE SYSTEM
Primary DI
08809763501852
Version / Model
14100
Company Name
BK MEDITECH CO.,LTD.
Labeler DUNS
687941818
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-23
Public Version
1
Public Version Date
2023-07-03
Public Version Status
New
Public Device Record Key
7358a9c9-8c1c-462b-898a-404d06593a92

Device Description

Long-Arm Breaker

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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FZT Cutter, Surgical

GMDN Terms

Code Name
44805 Orthopaedic implantable-device cutter

Identifiers

Type ID
Primary 08809763501852