FDA UDI In Commercial Distribution 🇺🇸 United States

Preat

DI: 00842092175606 · Model: 0102008 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Preat
Primary DI
00842092175606
Version / Model
0102008
Catalog Number
0102008
Company Name
Preat Corporation
Labeler DUNS
117776048
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2022-10-25
Public Version
6
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
98aa90ab-6102-471e-af50-fa132ebb4b45

Device Description

Preci Post Yellow Lab Refill

Device Characteristics

Single Use
Yes
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
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
63662 Dental implant suprastructure reamer

Identifiers

Type ID
Unit of Use 00842092175521
Primary 00842092175606

Customer Contacts