FDA UDI In Commercial Distribution 🇺🇸 United States

BellaTek

DI: 00844868043980 · Model: TF4122 · BIOMET 3I, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BellaTek
Primary DI
00844868043980
Version / Model
TF4122
Company Name
BIOMET 3I, LLC
Labeler DUNS
186127825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-05
Public Version
2
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
3f78d661-d548-4c76-853c-f927940899d8

Device Description

TSV® BELLATEK® FLEX ABUTMENT 4.5MM (D) 12MM (H) NON-HEXED

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
No
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
Primary 00844868043980

Device Sizes

Type Value Unit Text
Height 12 Millimeter
Outer Diameter 4.5 Millimeter