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Convertors

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CONVERTORS FDA UDI
Generic Name
Ophthalmic surgical drape FDA UDI
Device Name
Eyescape Ophthalmic Drape with Pouch FDA UDI
Model / Reference
9562 FDA UDI
Description
Eyescape Ophthalmic Drape with Pouch FDA UDI

Identifiers

Catalog Number
9562 FDA UDI
Primary DI / UDI-DI
10885380121333 FDA UDI
FDA Product Code
HMT FDA UDI
GMDN Term
Ophthalmic surgical drape FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Width — 77 Inch FDA UDI
Length — 110 Inch FDA UDI

Category: Ophthalmic surgical drape

Convertors by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical drape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI accd6d09-099a-43b9-8c8e-8cf5e3a55d9b 35 fields · synced Jun 8, 2026