FDA UDI In Commercial Distribution 🇺🇸 United States

CONELOG® Abutment Selection Kit

DI: E219C801110001 · Model: C8011.1000 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONELOG® Abutment Selection Kit
Primary DI
E219C801110001
Version / Model
C8011.1000
Catalog Number
C8011.1000
Company Name
ALTATEC GmbH
Labeler DUNS
322018193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-18
Public Version
1
Public Version Date
2023-08-28
Public Version Status
New
Public Device Record Key
6b853356-33f4-430e-b0bc-04075b4db3f0

Device Description

CONELOG® Abutment Selection Kit

Device Characteristics

Single Use
No
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
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
61640 Dental implant abutment analog, laboratory

Identifiers

Type ID
Primary E219C801110001

Customer Contacts

Phone
7609181857