Identity
- Trade Name
- SUPER-SNAP FDA UDI
- Generic Name
- Dental abrasive disk, reusable FDA UDI
- Device Name
- Super-Snap VIOLET (Medium) Double sided Mini 50pcs FDA UDI
- Model / Reference
- L522 FDA UDI
- Description
- Super-Snap VIOLET (Medium) Double sided Mini 50pcs FDA UDI
Identifiers
- Catalog Number
- L522 FDA UDI
- Primary DI / UDI-DI
- 04548162339447 FDA UDI
- FDA Product Code
- EHJ FDA UDI
- GMDN Term
- Dental abrasive disk, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental abrasive disk, reusable
Super-Snap by Shofu Dental Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Shofu Dental Corp.
Sources (1)
- FDA UDI 9f358ed5-bda2-4734-87e9-b648a2e6f431 36 fields · synced May 30, 2026