Identity
- Trade Name
- MEIBOMIAN GLAND EVALUATOR FDA UDI
- Generic Name
- Meibomian gland camera FDA UDI
- Device Name
- ASSEMBLY PKGD LIPISCAN - US FDA UDI
- Model / Reference
- DMI-1000 FDA UDI
- Description
- ASSEMBLY PKGD LIPISCAN - US FDA UDI
Identifiers
- Catalog Number
- 400000 FDA UDI
- Primary DI / UDI-DI
- 00859623006919 FDA UDI
- FDA Product Code
- HKI FDA UDI
- GMDN Term
- Meibomian gland camera FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1120 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
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
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: Meibomian gland camera
Meibomian Gland Evaluator by Tearscience, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Tearscience, Inc.
Sources (1)
- FDA UDI e51828f8-7e00-4277-9738-a6ba2031a567 36 fields · synced May 30, 2026