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SightChek Digital Phoropter

FDA UDI

Class I (US FDA UDI)

by Reichert Inc.

Identity

Trade Name
SightChek Digital Phoropter FDA UDI
Generic Name
Phoropter, electric FDA UDI
Model / Reference
16290 FDA UDI

Identifiers

Primary DI / UDI-DI
00812559012263 FDA UDI
FDA Product Code
HKN FDA UDI
GMDN Term
Phoropter, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1770 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Phoropter, electric

SightChek Digital Phoropter by Reichert Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phoropter, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reichert Inc.

Sources (1)

  • FDA UDI edba5008-245d-4bfc-84e5-5fb55524438d 32 fields · synced Jun 8, 2026