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Eye Shield

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
EYE SHIELD FDA UDI
Generic Name
Radiation/mechanical corneal shield, reusable FDA UDI
Device Name
EYE SHIELD WITH HANDLE BLUE ELECTRO COATED FDA UDI
Model / Reference
18-8022B FDA UDI
Description
EYE SHIELD WITH HANDLE BLUE ELECTRO COATED FDA UDI

Identifiers

Catalog Number
18-8022B FDA UDI
Primary DI / UDI-DI
00192896019607 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

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 343f11dc-4e6d-417c-9e8d-b75896b56d06 36 fields · synced Jun 1, 2026