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Digital Refractor

FDA UDI

Class I (US FDA UDI)

by Chongqing Yeasn Science & Technology Co., Ltd.

Identity

Trade Name
Digital Refractor FDA UDI
Generic Name
Phoropter, manual FDA UDI
Model / Reference
YPA-2100 FDA UDI

Identifiers

Catalog Number
YPA21/3 FDA UDI
Primary DI / UDI-DI
06971922132046 FDA UDI
FDA Product Code
HKN FDA UDI
GMDN Term
Phoropter, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1770 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Digital Refractor 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

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Manufacturer

Sources (1)

  • FDA UDI 49c202eb-43c6-4e55-8930-e6c068b38a1a 34 fields · synced May 30, 2026