FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00844868002130 · Model: DI2315 · BIOMET 3I, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00844868002130
Version / Model
DI2315
Company Name
BIOMET 3I, LLC
Labeler DUNS
186127825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-04
Public Version
5
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
29ade69d-e260-4048-9c71-440c1dc9f635

Device Description

DIRECTION INDICATOR, 2.3MM(D) X 15MM(L)

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NDP Accessories, implant, dental, endosseous

GMDN Terms

Code Name
31846 Dental implantation depth/angle gauge, reusable

Identifiers

Type ID
Primary 00844868002130

Customer Contacts

Device Sizes

Type Value Unit Text
Length 15 Millimeter
Device Size Text, specify Diameter 2.3 mm