FDA UDI In Commercial Distribution 🇺🇸 United States

Multi Unit Abutment for EX

DI: 07290112280701 · Model: MU-413EXN · DENTACK IMPLANTS LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Multi Unit Abutment for EX
Primary DI
07290112280701
Version / Model
MU-413EXN
Company Name
DENTACK IMPLANTS LTD
Labeler DUNS
514897185
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-26
Public Version
1
Public Version Date
2019-03-11
Public Version Status
New
Public Device Record Key
343104dc-56d4-4e18-b5c9-873f31a8e4c3

Device Description

Multi Unit Abutment for EX

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
DZE Implant, Endosseous, Root-Form
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 07290112280701

Customer Contacts

Phone
+97297660379

Premarket Submissions

Submission Number Supplement Number
K180859 000