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One Series Ultra

FDA UDI

Class I (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
ONE SERIES ULTRA FDA UDI
Generic Name
Intraocular lens-insertion cartridge FDA UDI
Device Name
ONE SERIES ULTRA CARTRIDGE 30/BOX FDA UDI
Model / Reference
1VIPR30 FDA UDI
Description
ONE SERIES ULTRA CARTRIDGE 30/BOX FDA UDI

Identifiers

Catalog Number
1VIPR30 FDA UDI
Primary DI / UDI-DI
05050474534605 FDA UDI
510(k) Number
K081545 FDA UDI
FDA Product Code
KYB FDA UDI
GMDN Term
Intraocular lens-insertion cartridge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4300 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intraocular lens-insertion cartridge

One Series Ultra by Johnson & Johnson Surgical Vision, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular lens-insertion cartridge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ecf75317-5a3a-43fb-8c5a-261b3fd1eac3 37 fields · synced Jun 9, 2026