FDA UDI In Commercial Distribution 🇺🇸 United States

ACT®

DI: 00844868042273 · Model: ACT3115SP · BIOMET 3I, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACT®
Primary DI
00844868042273
Version / Model
ACT3115SP
Company Name
BIOMET 3I, LLC
Labeler DUNS
186127825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-05
Public Version
3
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
7c905079-a544-4417-b5e2-652378bb972d

Device Description

SINGLE PATIENT ACT® TWIST DRILL, 3.15MM(D) X 15MM(L)

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
Yes
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
NDP Accessories, implant, dental, endosseous

GMDN Terms

Code Name
45697 Fixture/appliance dental drill bit, single-use

Identifiers

Type ID
Primary 00844868042273

Customer Contacts