FDA UDI In Commercial Distribution 🇺🇸 United States

MEDENTiKA

DI: EMKAI42009 · Model: I 4200 · MEDENTiKA GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
MEDENTiKA
Primary DI
EMKAI42009
Version / Model
I 4200
Catalog Number
I 4200
Company Name
MEDENTiKA GmbH
Labeler DUNS
537555497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-20
Public Version
3
Public Version Date
2022-11-14
Public Version Status
Update
Public Device Record Key
969d62b2-1e75-404d-8cfa-c0554a9700d8

Device Description

MedentiBASE abutment

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
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
Secondary 04251574818829
Primary EMKAI42009

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142167 000

Device Sizes

Type Value Unit Text
Device Size Text, specify compatible with BIOMET 3i / External Hex; D 3,4