FDA UDI In Commercial Distribution 🇺🇸 United States

2Shape Mini

DI: J015209532031 · Model: F35 n35 6% L21 Classics sterile · MICRO MEGA
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
2Shape Mini
Primary DI
J015209532031
Version / Model
F35 n35 6% L21 Classics sterile
Catalog Number
20953203
Company Name
MICRO MEGA
Labeler DUNS
276075371
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2022-09-21
Public Version
1
Public Version Date
2022-09-29
Public Version Status
New
Public Device Record Key
d5381ba9-7892-4e57-b1be-5d531329612f

Device Description

Endodontic instrument for professionnal dental use only

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EKS File, Pulp Canal, Endodontic

GMDN Terms

Code Name
40529 Rotary/reciprocating endodontic file/rasp, reusable

Identifiers

Type ID
Package J015209532039
Unit of Use J015209532030
Primary J015209532031

Storage Conditions

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