FDA UDI In Commercial Distribution 🇺🇸 United States

Esthet-X®flow Liquid Micro Hybrid

DI: D0026481131 · Model: 648113 · DENTSPLY INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Esthet-X®flow Liquid Micro Hybrid
Primary DI
D0026481131
Version / Model
648113
Catalog Number
648113
Company Name
DENTSPLY INTERNATIONAL INC.
Labeler DUNS
083235549
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2023-08-31
Public Version Status
Update
Public Device Record Key
4f088855-cd77-4832-b585-ba4eb4de6143

Device Description

Esthet-X®flow Liquid Micro Hybrid, A4, 20 Compula® Tips Refill Package

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EMA CEMENT, DENTAL

GMDN Terms

Code Name
35870 Dental composite resin

Identifiers

Type ID
Primary D0026481131
Unit of Use D0026481130

Customer Contacts

Device Sizes

Type Value Unit Text
Weight 0.25 Gram
Device Size Text, specify Esthet-X®flow Liquid Micro Hybrid A4, 20 Compula® Tips

Storage Conditions

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