FDA UDI In Commercial Distribution 🇺🇸 United States

EndoREZ

DI: 00883205107817 · Model: 5904 · ULTRADENT PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndoREZ
Primary DI
00883205107817
Version / Model
5904
Catalog Number
5904
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
2018-09-03
Public Version Status
Update
Public Device Record Key
29556bb0-ed7d-4a11-bea9-513b2b633993

Device Description

EndoREZ Mini Obturation Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
EFB HANDPIECE, AIR-POWERED, DENTAL

GMDN Terms

Code Name
36095 Endodontic filling/sealing material

Identifiers

Type ID
Primary 00883205107817

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K992380 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius