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Ocular Surface Analyzer

FDA UDI

Class II (US FDA UDI)

by Chongqing Sunkingdom Medical Instrument Co., Ltd

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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9bf81b98-9e77-4a8e-9f3f-277f4650dcec 32 fields · synced Jun 8, 2026