FDA UDI In Commercial Distribution 🇺🇸 United States

3i T3® DCD®

DI: 00844868028970 · Model: BNSS310 · BIOMET 3I, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3i T3® DCD®
Primary DI
00844868028970
Version / Model
BNSS310
Company Name
BIOMET 3I, LLC
Labeler DUNS
186127825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
d15e419b-1773-4ca6-9f95-1ddc1c545051

Device Description

3i T3® WITH DCD® NON-PLATFORM SWITCHED PARALLEL WALLED IMPLANT 3.25 X 10MM

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE IMPLANT, ENDOSSEOUS, ROOT-FORM

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 00844868028970

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10 Millimeter
Device Size Text, specify Diameter 3.25 mm