FDA UDI In Commercial Distribution 🇺🇸 United States

US SA Implant System

DI: 08800000968636 · Model: US2R4018S · 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
08800000968636
Version / Model
US2R4018S
Company Name
Osstem Implant Co., Ltd.
Labeler DUNS
689051793
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-02
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c258177e-09cc-40d7-9dad-629e4d08c4b9

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 08800000968636

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K161103 000