FDA UDI In Commercial Distribution 🇺🇸 United States

Zirlux

DI: H65890106790 · Model: 9010679 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zirlux
Primary DI
H65890106790
Version / Model
9010679
Catalog Number
9010679
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
16f4fb09-5044-4124-bb6a-76c782b708ab

Device Description

Zirlux Bite Ver Cyl Engage

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
Yes
PM Exempt
Yes
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
NDP ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
61648 Dental prosthesis bite verification device

Identifiers

Type ID
Primary H65890106790