Identity
- Trade Name
- Eighteeth FDA UDI
- Generic Name
- Hand-held intraoral dental x-ray system, digital FDA UDI
- Device Name
- The HyperLight Hand-held Dental X-ray System is indicated for use only by a trained and qualified dentist or dental technician for both adult and pediatric subjects as an extraoral diagnostic dental X-ray source to produce X-ray images using intraoral image receptors. This device must only be used in hospital environments, clinics or dental offices where appropriate safeguards are implemented, and not used in the oxygen-rich environment. FDA UDI
- Model / Reference
- HyperLight FDA UDI
- Description
- The HyperLight Hand-held Dental X-ray System is indicated for use only by a trained and qualified dentist or dental technician for both adult and pediatric subjects as an extraoral diagnostic dental X-ray source to produce X-ray images using intraoral image receptors. This device must only be used in hospital environments, clinics or dental offices where appropriate safeguards are implemented, and not used in the oxygen-rich environment. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06941877803193 FDA UDI
- 510(k) Number
- K232068 FDA UDI
- FDA Product Code
- EHD FDA UDI
- GMDN Term
- Hand-held intraoral dental x-ray system, digital FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.1800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Hand-held intraoral dental x-ray system, digital
Eighteeth by Changzhou Sifary Medical Technology Co., Ltd. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Changzhou Sifary Medical Technology Co., Ltd.
Sources (1)
- FDA UDI 093965eb-de94-42a3-b3c6-339751982444 34 fields · synced May 30, 2026