FDA UDI In Commercial Distribution 🇺🇸 United States

MEDENTiKA

DI: 04251574854711 · Model: NE 40 RK · MEDENTiKA GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDENTiKA
Primary DI
04251574854711
Version / Model
NE 40 RK
Catalog Number
NE 40 RK
Company Name
MEDENTiKA GmbH
Labeler DUNS
537555497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-23
Public Version
1
Public Version Date
2022-03-03
Public Version Status
New
Public Device Record Key
4a37c678-52e8-48a9-ab4c-87e8710e2fa9

Device Description

Drilling sleeve

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
57789 Surgical drill guide, single-use

Identifiers

Type ID
Secondary EMKANE40RK9
Primary 04251574854711

Device Sizes

Type Value Unit Text
Device Size Text, specify NEOSS ProActive Tapered