FDA UDI In Commercial Distribution 🇺🇸 United States

Wax Denture

DI: 08800049310014 · Model: WDU 02 · DIO Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Wax Denture
Primary DI
08800049310014
Version / Model
WDU 02
Company Name
DIO Corporation
Labeler DUNS
631085206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
062eb4d7-b14c-467c-acdf-0ef0aed813e7

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EGD Wax, Dental, Intraoral

GMDN Terms

Code Name
16350 Dental impression tray, single-use

Identifiers

Type ID
Primary 08800049310014