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Ultracell®

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Ultracell® FDA UDI
Generic Name
Ophthalmic sponge FDA UDI
Device Name
***NON-STERILE*** INSTRUMENT WIPE, 3 X 3 X 2MM (300/SP) FDA UDI
Model / Reference
NS90900Z FDA UDI
Description
***NON-STERILE*** INSTRUMENT WIPE, 3 X 3 X 2MM (300/SP) FDA UDI

Identifiers

Catalog Number
NS90900Z FDA UDI
Primary DI / UDI-DI
30886158012093 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Ophthalmic sponge 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic sponge

Ultracell® by Beaver-Visitec International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic sponge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beaver-Visitec International, Inc.

Sources (1)

  • FDA UDI 11c1f47d-3a3a-4adc-89e1-195df683026a 36 fields · synced Jun 8, 2026