FDA UDI
In Commercial Distribution
🇺🇸 United States
EsCom 100 A3 Capsules
DI: 08809262955460
·
Model: 101-0603
·
Spident Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
6
Pkg Device Count
1
Basic Information
- Brand Name
- EsCom 100 A3 Capsules
- Primary DI
- 08809262955460
- Version / Model
- 101-0603
- Catalog Number
- 101-0603
- Company Name
- Spident Co., Ltd.
- Labeler DUNS
- 689370711
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-08-23
- Public Version
- 6
- Public Version Date
- 2023-05-05
- Public Version Status
- Update
- Public Device Record Key
- 1a3d85e0-94d9-488a-81e7-7e28ef7bb8d2
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 | 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 |
|---|---|---|---|---|---|---|
| Package | 20190723160274 | GS1 | 300 | Not in Commercial Distribution | 2019-05-16 | |
| Primary | 08809262955460 | GS1 | ||||
| Package | 00202202250089 | GS1 | 140 | Not in Commercial Distribution | 2021-01-25 | |
| Package | 00220305190231 | GS1 | 140 | Not in Commercial Distribution | 2021-01-25 | |
| Package | 00000202210276 | GS1 | 50 | Not in Commercial Distribution | 2022-10-27 | |
| Package | 00000202305057 | GS1 | 70 | Not in Commercial Distribution | 2023-05-05 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K110428 | 000 |