FDA UDI In Commercial Distribution 🇺🇸 United States

OSSEOTITE NT®

DI: 00844868012566 · Model: NTDIK · BIOMET 3I, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OSSEOTITE NT®
Primary DI
00844868012566
Version / Model
NTDIK
Company Name
BIOMET 3I, LLC
Labeler DUNS
186127825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-24
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
15847574-b833-42fc-a94d-66c72a8ad33a

Device Description

OSSEOTITE NT® DIRECTION/DEPTH INDICATOR KIT

Device Characteristics

Single Use
No
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
Yes
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
No

Product Codes

Code Name
NDP ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44883 Dental implant/prosthesis surgical procedure kit

Identifiers

Type ID
Primary 00844868012566

Customer Contacts