FDA UDI In Commercial Distribution 🇺🇸 United States

Titanium Non-Engaging Temporary Abutment

DI: 10841307114017 · Model: 6060-49 · IMPLANT DIRECT SYBRON MANUFACTURING LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titanium Non-Engaging Temporary Abutment
Primary DI
10841307114017
Version / Model
6060-49
Catalog Number
6060-49
Company Name
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Labeler DUNS
868856969
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
ff5e4163-dafa-42bd-ae2d-b444eb154961

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
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
No
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
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 10841307114017

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081101 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Platform: 6.0mm