FDA UDI In Commercial Distribution 🇺🇸 United States

K-Reamers

DI: J015600298481 · Model: N015/040 L31 · MICRO MEGA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
K-Reamers
Primary DI
J015600298481
Version / Model
N015/040 L31
Catalog Number
60029848
Company Name
MICRO MEGA
Labeler DUNS
276075371
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-22
Public Version
1
Public Version Date
2020-12-30
Public Version Status
New
Public Device Record Key
8a645c4d-0d0d-4383-8960-2b01723d3cde

Device Description

Endodontic instrument for professional dental use only

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKP Reamer, Pulp Canal, Endodontic

GMDN Terms

Code Name
31878 Manual endodontic file/rasp, reusable

Identifiers

Type ID
Package J015600298489
Primary J015600298481

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight