FDA UDI In Commercial Distribution 🇺🇸 United States

US SA Implant System

DI: 08800040640462 · Model: AUS3P5007S · Osstem Implant Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
US SA Implant System
Primary DI
08800040640462
Version / Model
AUS3P5007S
Company Name
Osstem Implant Co., Ltd.
Labeler DUNS
689051793
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-07
Public Version
1
Public Version Date
2022-02-15
Public Version Status
New
Public Device Record Key
eb54431f-2707-4f24-8f25-d797c986d1be

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 08800040640462

Premarket Submissions

Submission Number Supplement Number
K161103 000