FDA UDI In Commercial Distribution 🇺🇸 United States

Centurion

DI: 10653160351382 · Model: I68330K · CENTURION MEDICAL PRODUCTS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Centurion
Primary DI
10653160351382
Version / Model
I68330K
Catalog Number
I68330K
Company Name
CENTURION MEDICAL PRODUCTS CORPORATION
Labeler DUNS
017246562
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-21
Public Version
1
Public Version Date
2022-03-29
Public Version Status
New
Public Device Record Key
dbdfb7ad-144d-4bea-9edc-3c29edc3876f

Device Description

STERILE REPROCESSED BRUNS CURETTE #2

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HTF CURETTE

GMDN Terms

Code Name
62558 General-purpose curette

Identifiers

Type ID
Package 00653160351385
Primary 10653160351382

Customer Contacts