FDA UDI In Commercial Distribution 🇺🇸 United States

Centurion, OZil

DI: 00380657517619 · Model: 8065751761 · Alcon Laboratories, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Centurion, OZil
Primary DI
00380657517619
Version / Model
8065751761
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-06
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
53996700-9a83-432e-b9df-34f2a7e22166

Device Description

Centurion Ozil Handpiece

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
HQE Instrument, vitreous aspiration and cutting, ac-powered
HQC Unit, phacofragmentation

GMDN Terms

Code Name
34900 Phacoemulsification system handpiece

Identifiers

Type ID
Primary 00380657517619

Customer Contacts