FDA UDI In Commercial Distribution 🇺🇸 United States

REVO-S

DI: J015209431571 · Model: SC2 L21 · MICRO MEGA
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
REVO-S
Primary DI
J015209431571
Version / Model
SC2 L21
Catalog Number
20943157
Company Name
MICRO MEGA
Labeler DUNS
276075371
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-08-28
Public Version
1
Public Version Date
2020-09-07
Public Version Status
New
Public Device Record Key
29ba3580-4ef5-4330-a9f2-06a3b77b9186

Device Description

Endodontic instrument for professionnal 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
EKS File, Pulp Canal, Endodontic

GMDN Terms

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

Identifiers

Type ID
Package J015209431579
Primary J015209431571
Unit of Use J015209431570

Storage Conditions

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