FDA UDI In Commercial Distribution 🇺🇸 United States

Astra

DI: 00842092102428 · Model: 8002135 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Astra
Primary DI
00842092102428
Version / Model
8002135
Catalog Number
8002135
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
5
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
2ca1d9be-968b-4a34-a6f3-479144a1a876

Device Description

Astra®-compatible Aqua 3.5/4.0mm Non-Engaging Verification Cylinder

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
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
Package 00842092162781
Primary 00842092102428

Customer Contacts