FDA UDI In Commercial Distribution 🇺🇸 United States

DENTIOIII series

DI: 08800005200113 · Model: DENTIOIII · HDX WILL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DENTIOIII series
Primary DI
08800005200113
Version / Model
DENTIOIII
Company Name
HDX WILL CORP.
Labeler DUNS
689605054
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-04
Public Version
3
Public Version Date
2022-01-06
Public Version Status
Update
Public Device Record Key
660c1596-0455-4a9a-ba78-8c7f1b850b20

Device Description

The DENTIOIII is intended for dental radiographic examination of the teeth and temporomandibular joints, specifically for panoramic examinations. It is to be used only by dental practitioners and/or radiologists.

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MUH System, X-Ray, Extraoral Source, Digital

GMDN Terms

Code Name
43369 Stationary panoramic dental x-ray system, digital

Identifiers

Type ID
Primary 08800005200113

Customer Contacts

Phone
+82215882754

Premarket Submissions

Submission Number Supplement Number
K181297 000