Identity
- Trade Name
- YEASN FDA UDI
- Generic Name
- Manually-adjusted lensmeter, line-powered FDA UDI
- Model / Reference
- CCQ-800 FDA UDI
Identifiers
- Catalog Number
- CCQ8/10 FDA UDI
- Primary DI / UDI-DI
- 06971922131070 FDA UDI
- FDA Product Code
- HLM FDA UDI
- GMDN Term
- Manually-adjusted lensmeter, line-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1425 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Yeasn by Chongqing Yeasn Science & Technology Co., Ltd. — 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 |
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Manufacturer
- Manufacturer
- Chongqing Yeasn Science & Technology Co., Ltd.
Sources (1)
- FDA UDI 6e1633e6-c616-4ff3-af36-58bab224c8fa 34 fields · synced May 30, 2026