FDA UDI In Commercial Distribution 🇺🇸 United States

Roydent

DI: D8095021 · Model: 502 · ROYDENT DENTAL PRODUCTS INC
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
Roydent
Primary DI
D8095021
Version / Model
502
Catalog Number
502
Company Name
ROYDENT DENTAL PRODUCTS INC
Labeler DUNS
131487225
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-07
Public Version
3
Public Version Date
2021-10-29
Public Version Status
Update
Public Device Record Key
f5057a9b-3edc-4aab-80b3-59dcd41200ec

Device Description

REFORM TEMP. C&B MATERIAL A3.5

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EBG CROWN AND BRIDGE, TEMPORARY, RESIN

GMDN Terms

Code Name
31783 Temporary dental crown/bridge

Identifiers

Type ID
Primary D8095021

Customer Contacts

Device Sizes

Type Value Unit Text
Weight 74 Gram

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a Cool Dry Place