FDA UDI In Commercial Distribution 🇺🇸 United States

CONELOG® Disconnector for CONELOG® Abutments

DI: E219C530016031 · Model: C5300.1603 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONELOG® Disconnector for CONELOG® Abutments
Primary DI
E219C530016031
Version / Model
C5300.1603
Catalog Number
C5300.1603
Company Name
ALTATEC GmbH
Labeler DUNS
322018193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-31
Public Version
1
Public Version Date
2019-01-31
Public Version Status
New
Public Device Record Key
578af925-e3e6-4280-92a0-009fa8f88003

Device Description

CONELOG® Disconnector for CONELOG® Abutments, thread M1.6, long

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary E219C530016031

Customer Contacts

Phone
9999999999