FDA UDI In Commercial Distribution 🇺🇸 United States

DIOnavi-C&B Z

DI: 08800049401507 · Model: 3DCNBF-1000B3 · DIO Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DIOnavi-C&B Z
Primary DI
08800049401507
Version / Model
3DCNBF-1000B3
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
4f2df099-a0fd-4704-ad86-e7bc57730cf1

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
38781 Dental prosthesis veneer resin

Identifiers

Type ID
Primary 08800049401507