FDA UDI In Commercial Distribution 🇺🇸 United States

Genie MagicMix® Ultra Hydrophilic Impression Standard

DI: D6870078835FG1 · Model: 0078835FG · DENTSPLY INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
Genie MagicMix® Ultra Hydrophilic Impression Standard
Primary DI
D6870078835FG1
Version / Model
0078835FG
Catalog Number
0078835FG
Company Name
DENTSPLY INTERNATIONAL INC.
Labeler DUNS
083235549
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2016-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
41517597-4a2e-4014-b160-40a8f22f3bac

Device Description

Genie MagicMix Heavy Body Standard Set Bulk

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
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
ELW MATERIAL, IMPRESSION

GMDN Terms

Code Name
35866 Silicone dental impression material

Identifiers

Type ID
Primary D6870078835FG1
Unit of Use D6870078835FG0

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 380 Milliliter
Device Size Text, specify Genie MagicMix® Heavy Body Standard Set (4) 380 mL cartridges and 1 Bayonet Ring

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 27 Degrees Celsius