FDA UDI In Commercial Distribution 🇺🇸 United States

Preat

DI: 00842092182222 · Model: 9001664 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Preat
Primary DI
00842092182222
Version / Model
9001664
Catalog Number
9001664
Company Name
Preat Corporation
Labeler DUNS
117776048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-09
Public Version
2
Public Version Date
2024-07-23
Public Version Status
Update
Public Device Record Key
1cf5fd7b-438a-442a-aba3-16e1f1e19136

Device Description

ASC Biomet 3i Certain®-compatible 3.4mm Non-Engaging Titanium Base

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 Unsafe
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
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary 00842092182222

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183518 000