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Corneal Eye Shield

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
CORNEAL EYE SHIELD FDA UDI
Generic Name
Radiation/mechanical corneal shield, reusable FDA UDI
Device Name
CORNEAL EYE SHIELD LARGE SIZE GREEN PLASTIC FDA UDI
Model / Reference
1100-409LG FDA UDI
Description
CORNEAL EYE SHIELD LARGE SIZE GREEN PLASTIC FDA UDI

Identifiers

Catalog Number
1100-409LG FDA UDI
Primary DI / UDI-DI
00192896047433 FDA UDI
FDA Product Code
MOE FDA UDI
GMDN Term
Radiation/mechanical corneal shield, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4750 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiation/mechanical corneal shield, reusable

Corneal Eye Shield by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation/mechanical corneal shield, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c620bd06-87da-4bc8-a201-d26f232ac875 35 fields · synced May 31, 2026