FDA UDI In Commercial Distribution 🇺🇸 United States

DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM

DI: 08800049287828 · Model: STI 2004 · DIO Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM
Primary DI
08800049287828
Version / Model
STI 2004
Catalog Number
STI 2004
Company Name
DIO Corporation
Labeler DUNS
631085206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-01
Public Version
1
Public Version Date
2022-03-09
Public Version Status
New
Public Device Record Key
2466d41b-3839-4b3f-b1cd-f86ee3314dda

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 08800049287828

Premarket Submissions

Submission Number Supplement Number
K170608 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
1 – 30 Degrees Celsius