FDA UDI In Commercial Distribution 🇺🇸 United States

MEDENTiKA

DI: EMKAF1310 · Model: F 1310 · MEDENTiKA GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEDENTiKA
Primary DI
EMKAF1310
Version / Model
F 1310
Company Name
MEDENTiKA GmbH
Labeler DUNS
537555497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-07
Public Version
4
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
809b655f-5859-4c85-9ee7-61c7c7b07dfd

Device Description

Titanium Base

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
MR Conditional
Direct Marking Exempt
Yes
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
No

Product Codes

Code Name
NHA ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary EMKAF1310

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Compatible with implant system: Nobel Active Implant; RP 4,3/5,0
Height 5.5 Millimeter