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Us Professional Complete Led Student Set

FDA UDI

Class II (US FDA UDI)

by Keeler Limited

Identity

Trade Name
US PROFESSIONAL COMPLETE LED STUDENT SET FDA UDI
Generic Name
Retinoscope, line-powered FDA UDI
Model / Reference
1427-P-1127-500 FDA UDI

Identifiers

Primary DI / UDI-DI
05055272719971 FDA UDI
FDA Product Code
HKL FDA UDI
GMDN Term
Retinoscope, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1780 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Retinoscope, line-powered

Us Professional Complete Led Student Set by Keeler Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Retinoscope, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keeler Limited

Sources (1)

  • FDA UDI b28088eb-78a5-4852-9513-11a799c1637c 32 fields · synced Jun 8, 2026