FDA UDI In Commercial Distribution 🇺🇸 United States

ArgenIS

DI: D818115303 · Model: DX 3.8 Ti Blank · ARGEN CORPORATION, THE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ArgenIS
Primary DI
D818115303
Version / Model
DX 3.8 Ti Blank
Catalog Number
115303
Company Name
ARGEN CORPORATION, THE
Labeler DUNS
103095543
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-17
Public Version
1
Public Version Date
2023-01-25
Public Version Status
New
Public Device Record Key
700b4cd7-0e85-475a-a52d-10001463e9a8
Distribution End Date
2027-01-16

Device Description

DX 3.8 Ti Blank

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
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
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
61647 Dental prosthesis/implant abutment screw

Identifiers

Type ID
Primary D818115303

Premarket Submissions

Submission Number Supplement Number
K173908 000