FDA UDI Not in Commercial Distribution 🇺🇸 United States

Qu-resin dentin

DI: EBRE580012660 · Model: 58001266 · bredent GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Qu-resin dentin
Primary DI
EBRE580012660
Version / Model
58001266
Catalog Number
58001266
Company Name
bredent GmbH & Co. KG
Labeler DUNS
341086190
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-07
Public Version
2
Public Version Date
2025-04-02
Public Version Status
Update
Public Device Record Key
efc965c2-2c89-49c2-a6ff-b2f694813520
Distribution End Date
2024-05-27

Device Description

Qu-resin dentin 6ml Cartridge 1 Piece

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKO Denture preformed (partially prefabricated denture)

GMDN Terms

Code Name
35870 Dental composite resin

Identifiers

Type ID
Package EBRE580012669
Primary EBRE580012660

Customer Contacts