FDA UDI
In Commercial Distribution
🇺🇸 United States
CLEARFIL™ DC CORE PLUS
DI: EKUR001030KA1
·
Model: #1030-KA
·
KURARAY NORITAKE DENTAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20
Basic Information
- Brand Name
- CLEARFIL™ DC CORE PLUS
- Primary DI
- EKUR001030KA1
- Version / Model
- #1030-KA
- Company Name
- KURARAY NORITAKE DENTAL INC.
- Labeler DUNS
- 697119498
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 20
- Record Status
- Published
- Publish Date
- 2017-02-17
- Public Version
- 4
- Public Version Date
- 2021-08-10
- Public Version Status
- Update
- Public Device Record Key
- a634dcb4-e4c2-4738-81d9-3c3749093210
Device Description
Guide tip (S)
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
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| EBF | Material, Tooth Shade, Resin | Dental | 872.3690 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 35870 | Dental composite resin | A non-sterile substance intended for professional use as a dental luting agent, liner, base, pulp-capping material, pit/fissure sealant, and/or direct dental restorative material, whereby the majority of the setting reaction is based on the self-, light-, or dual-cured polymerization of a dimethacrylate resin [e.g., polymethylmethacrylate (PMMA), polyurethane, or bisphenol-A-diglycidylether methacrylate (Bis-GMA)]; it includes some additional fillers/components (e.g., glass-based, quartz, or ceramic). It may be preloaded into a syringe, and dedicated disposable devices associated with application may be included. After application, this device cannot be reused. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | EKUR001030KA1 | HIBCC | ||||
| Unit of Use | EKUR001030KA0 | HIBCC |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K111982 | 000 |