FDA UDI In Commercial Distribution 🇺🇸 United States

Ultra-Blend Plus

DI: 00883205103604 · Model: 416 · ULTRADENT PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ultra-Blend Plus
Primary DI
00883205103604
Version / Model
416
Catalog Number
416
Company Name
ULTRADENT PRODUCTS, INC.
Labeler DUNS
013369913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a4d76785-bf1b-4832-a2ee-128b73a8d1a8

Device Description

Ultra-Blend Plus Dentin Refill

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
No
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
EJK LINER, CAVITY, CALCIUM HYDROXIDE

GMDN Terms

Code Name
62199 Calcium hydroxide dental cement

Identifiers

Type ID
Primary 00883205103604

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K970113 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius