FDA UDI In Commercial Distribution 🇺🇸 United States

Preat

DI: 00842092182789 · Model: 9006753 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Preat
Primary DI
00842092182789
Version / Model
9006753
Catalog Number
9006753
Company Name
Preat Corporation
Labeler DUNS
117776048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-10
Public Version
1
Public Version Date
2025-06-18
Public Version Status
New
Public Device Record Key
d1e8e6e6-4f01-4ace-88b6-c8aa7bfec30b

Device Description

ASC Astra EV 4.8mm/5.4mm-Compatible Titanium 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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
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
NHA Abutment, implant, dental, endosseous

GMDN Terms

Code Name
61647 Dental prosthesis/implant abutment screw

Identifiers

Type ID
Primary 00842092182789

Customer Contacts