Identity
- Trade Name
- Ocular Surface Analyzer FDA UDI
- Generic Name
- Meibomian gland camera/ophthalmic interferometer FDA UDI
- Model / Reference
- DA-2 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06973211070770 FDA UDI
- FDA Product Code
- PUE FDA UDI
- GMDN Term
- Meibomian gland camera/ophthalmic interferometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1850 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Meibomian gland camera/ophthalmic interferometer
Ocular Surface Analyzer by Chongqing Sunkingdom Medical Instrument Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Meibomian gland camera/ophthalmic interferometer.
- LIPIVIEW II OCULAR SURFACE INTERFEROMETE — TEARSCIENCE, INC. · Class II
- MOPTIM — Shenzhen CERTAINN Technology Co., Ltd. · Class I
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
- Chongqing Sunkingdom Medical Instrument Co., Ltd
Sources (1)
- FDA UDI 9bf81b98-9e77-4a8e-9f3f-277f4650dcec 32 fields · synced Jun 8, 2026