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Atlanta Healthcare Services Ocudrape

FDA UDI

Class I (US FDA UDI)

by Atlanta Healthcare Services

Identity

Trade Name
Atlanta Healthcare Services Ocudrape FDA UDI
Generic Name
Postsurgical eye shield, vented FDA UDI
Device Name
Eye Shield, Polycarbonate, Optical Grade for Clarity & Safety, BPA Free, 100 / BOX, Non Sterile FDA UDI
Model / Reference
10851736007996 FDA UDI
Description
Eye Shield, Polycarbonate, Optical Grade for Clarity & Safety, BPA Free, 100 / BOX, Non Sterile FDA UDI

Identifiers

Catalog Number
OES5702CS FDA UDI
Primary DI / UDI-DI
10851736007996 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Postsurgical eye shield, vented

Atlanta Healthcare Services Ocudrape by Atlanta Healthcare Services — 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 f11f8bbe-bbbc-4801-a3b0-5a4378c1f379 35 fields · synced Jun 8, 2026