FDA UDI In Commercial Distribution 🇺🇸 United States

TriRock Dental

DI: D170830012MTRD1002 · Model: 830-012M · TriRock Dental LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
TriRock Dental
Primary DI
D170830012MTRD1002
Version / Model
830-012M
Catalog Number
830-012M-TRD-100
Company Name
TriRock Dental LLC
Labeler DUNS
118701065
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-12-05
Public Version
1
Public Version Date
2025-12-15
Public Version Status
New
Public Device Record Key
71fb578f-eca5-44c9-9add-85eb29ea7cdf

Device Description

TriRockDental FG #830-012M Diamond

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
DZP INSTRUMENT, DIAMOND, DENTAL

GMDN Terms

Code Name
45525 Diamond dental bur, single-use

Identifiers

Type ID
Unit of Use D170830012MTRD1000
Primary D170830012MTRD1002

Customer Contacts