FDA UDI In Commercial Distribution 🇺🇸 United States

CONELOG® Temporary abutment

DI: E219C223933001 · Model: C2239.3300 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONELOG® Temporary abutment
Primary DI
E219C223933001
Version / Model
C2239.3300
Catalog Number
C2239.3300
Company Name
ALTATEC GmbH
Labeler DUNS
322018193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
80d040e0-a345-4c83-b33d-024eb6bd9d78

Device Description

C2239.3300 CONELOG® Temporary abutment (titanium) d 3.3 mm

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
No
PM Exempt
No
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
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

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

Identifiers

Type ID
Primary E219C223933001

Customer Contacts

Phone
7609181857