FDA UDI In Commercial Distribution 🇺🇸 United States

CONELOG® Esthomic® abutment

DI: E219C223233151 · Model: C2232.3315 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONELOG® Esthomic® abutment
Primary DI
E219C223233151
Version / Model
C2232.3315
Catalog Number
C2232.3315
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
4
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
48544561-a426-4b46-88c2-fce76a938da9

Device Description

C2232.3315 CONELOG® Esthomic abutment®, 20deg, Type B, d 3.3, GH 1.5-2.5 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
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary E219C223233151

Customer Contacts

Phone
7609181857