FDA UDI In Commercial Distribution 🇺🇸 United States

Preat

DI: 00842092109229 · Model: 0807500 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Preat
Primary DI
00842092109229
Version / Model
0807500
Catalog Number
0807500
Company Name
Preat Corporation
Labeler DUNS
117776048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-24
Public Version
4
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
156a1ac5-7fc2-4576-8fee-a08f71ef4f5d

Device Description

CSA Paralleling Mandrel

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NDP Accessories, implant, dental, endosseous

GMDN Terms

Code Name
35170 Dental mandrel

Identifiers

Type ID
Primary 00842092109229

Customer Contacts