FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: 08809985659508 · Model: AXSB502 · Megagen Implant Co. Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Scan Bar
Primary DI
08809985659508
Version / Model
AXSB502
Catalog Number
AXSB502T
Company Name
Megagen Implant Co. Ltd
Labeler DUNS
687388178
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-10
Public Version
1
Public Version Date
2024-07-18
Public Version Status
New
Public Device Record Key
4307326d-8714-45af-9fac-b8fc87ef4698

Device Description

Common

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
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
64355 Dental implant abutment trial

Identifiers

Type ID
Primary 08809985659508