← Back to catalogue

Eye Shield With Handle

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Eye Shield With Handle FDA UDI
Generic Name
Radiation/mechanical corneal shield, reusable FDA UDI
Device Name
Eye Shield With Handle Child Size 24 x 21 Millimeter One Each Titanium FDA UDI
Model / Reference
T18-8023 FDA UDI
Description
Eye Shield With Handle Child Size 24 x 21 Millimeter One Each Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
00192896114739 FDA UDI
FDA Product Code
HOY 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 With Handle 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 21e32aeb-bcec-43d5-81d6-18d7f78cef85 34 fields · synced May 30, 2026