FDA UDI In Commercial Distribution 🇺🇸 United States

3i Certain®-compatible

DI: 00842092181928 · Model: 9001803 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
3i Certain®-compatible
Primary DI
00842092181928
Version / Model
9001803
Catalog Number
9001803
Company Name
Preat Corporation
Labeler DUNS
117776048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-06
Public Version
1
Public Version Date
2024-02-14
Public Version Status
New
Public Device Record Key
30f7de47-a958-4bb3-bdd1-b97140230fbe

Device Description

3i Certain®-compatible 5.0MM Digital Analog Kit contains: 1 3i Certain®-compatible 5.0MM Digital Analog 1 Digital Analog Base Screw

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
61641 Dental implant abutment analog, scanning

Identifiers

Type ID
Package 00842092181935
Primary 00842092181928

Customer Contacts