Identity
- Trade Name
- Mirror Magic® FDA UDI
- Generic Name
- Dental antifog solution FDA UDI
- Device Name
- "Mirror Magic Trial Kit 2 x 6mL Anti-Fog Solution 24 x Swipe Pads" FDA UDI
- Model / Reference
- 50R200 FDA UDI
- Description
- "Mirror Magic Trial Kit 2 x 6mL Anti-Fog Solution 24 x Swipe Pads" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840161308092 FDA UDI
- FDA Product Code
- EAX FDA UDI
- GMDN Term
- Dental antifog solution FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 95 Millimeter FDA UDIWidth — 92 Millimeter FDA UDIHeight — 48 Millimeter FDA UDI
Category: Dental antifog solution
Mirror Magic® by Zirc Dental Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Zirc Dental Products, Inc.
Sources (1)
- FDA UDI 9fd47ce4-7c41-4d4c-85b6-5e37f3705afc 34 fields · synced Jun 8, 2026