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Yeasn

FDA UDI

Class I (US FDA UDI)

by Chongqing Yeasn Science & Technology Co., Ltd.

Identity

Trade Name
YEASN FDA UDI
Generic Name
Manually-adjusted lensmeter, line-powered FDA UDI
Model / Reference
CCQ-400 FDA UDI

Identifiers

Catalog Number
CCQ4/41 FDA UDI
Primary DI / UDI-DI
06971922131728 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
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

Category: Manually-adjusted lensmeter, line-powered

Yeasn by Chongqing Yeasn Science & Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manually-adjusted lensmeter, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22b866c6-4168-4be0-826b-6999541dc98e 33 fields · synced Jun 8, 2026