FDA UDI In Commercial Distribution 🇺🇸 United States

Magic Motion

DI: 08800039399494 · Model: M32080 · InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Magic Motion
Primary DI
08800039399494
Version / Model
M32080
Company Name
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
Labeler DUNS
631169224
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-17
Public Version
1
Public Version Date
2020-06-25
Public Version Status
New
Public Device Record Key
68626dcd-e990-4d1a-8f21-59588c6821bc

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
55847 Dental implant system

Identifiers

Type ID
Primary 08800039399494

Premarket Submissions

Submission Number Supplement Number
K200753 000