FDA UDI In Commercial Distribution 🇺🇸 United States

Zirlux

DI: H65890122500 · Model: 9012250 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zirlux
Primary DI
H65890122500
Version / Model
9012250
Catalog Number
9012250
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
3
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
83cfa7a1-fcab-491d-8172-13b56b93a95d

Device Description

Zirlux UCLA Plastic Abutment compatible with: Straumann Tissue Level WN synOcta

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
No

Product Codes

Code Name
NDP ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary H65890122500

Device Sizes

Type Value Unit Text
Device Size Text, specify Post Height, 10mm