FDA UDI In Commercial Distribution 🇺🇸 United States

MEDENTiKA

DI: EMKAT91059 · Model: T 9105 · MEDENTiKA GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
MEDENTiKA
Primary DI
EMKAT91059
Version / Model
T 9105
Catalog Number
T 9105
Company Name
MEDENTiKA GmbH
Labeler DUNS
537555497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-08
Public Version
1
Public Version Date
2020-04-16
Public Version Status
New
Public Device Record Key
58fd95c7-4ef5-4ab4-bce8-5e0b46483f43

Device Description

MedentiCAD wax-up base

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
46122 Dental implant suprastructure, temporary, preformed, reusable

Identifiers

Type ID
Secondary 04251574831194
Primary EMKAT91059

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify compatible with DENTSPLY Implants / XiVE®* S