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Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Automated ophthalmic refractometer FDA UDI
Device Name
Welch Allyn SureSight Vision Screener; Automatically screens for common vision problems, including near and farsightedness (myopia/hyperopia), astigmatism (asymmetrical focus), and anisometropia (unequal power between eyes); Left/Right Difference Mode, Charging Base; 230 V, 50 Hz AC, Lithium-Ion (#72420) Battery; IEC Plug Type-E/F FDA UDI
Model / Reference
901029 FDA UDI
Description
Welch Allyn SureSight Vision Screener; Automatically screens for common vision problems, including near and farsightedness (myopia/hyperopia), astigmatism (asymmetrical focus), and anisometropia (unequal power between eyes); Left/Right Difference Mode, Charging Base; 230 V, 50 Hz AC, Lithium-Ion (#72420) Battery; IEC Plug Type-E/F FDA UDI

Identifiers

Catalog Number
14002 FDA UDI
Primary DI / UDI-DI
00732094088427 FDA UDI
FDA Product Code
HKO FDA UDI
GMDN Term
Automated ophthalmic refractometer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1760 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Welch Allyn, Inc. by Welch Allyn, Inc. — 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

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI fa32e463-7507-4edc-93d4-55bb1bcc5603 36 fields · synced Jun 8, 2026