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Pro-Paks

FDA UDI

Class I (US FDA UDI)

by Microspecialities, Inc.

Identity

Trade Name
Pro-Paks FDA UDI
Generic Name
Postsurgical eye shield, vented FDA UDI
Device Name
Universal Eye Shield, 100 per bag FDA UDI
Model / Reference
PO-ES FDA UDI
Description
Universal Eye Shield, 100 per bag FDA UDI

Identifiers

Catalog Number
PO-ES FDA UDI
Primary DI / UDI-DI
10810003224474 FDA UDI
FDA Product Code
HOY FDA UDI
GMDN Term
Postsurgical eye shield, vented 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Postsurgical eye shield, vented

Pro-Paks by Microspecialities, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Postsurgical eye shield, vented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30ac7e0c-0cda-43f9-9612-f8b75ec461c9 35 fields · synced May 30, 2026