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Sponge

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Sponge FDA UDI
Generic Name
Retina illumination shield FDA UDI
Device Name
INSTRUMENT WIPE & CORNEAL SHIELD BX/20 FDA UDI
Model / Reference
K20-5040 FDA UDI
Description
INSTRUMENT WIPE & CORNEAL SHIELD BX/20 FDA UDI

Identifiers

Catalog Number
K20-5040 FDA UDI
Primary DI / UDI-DI
10841668111946 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Retina illumination shield FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Retina illumination shield

Sponge by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Retina illumination shield.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katena Products, Inc.

Sources (1)

  • FDA UDI 7259cb3d-fe10-49f8-8ced-676360df07cb 35 fields · synced Jun 12, 2026