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Fs Disposable Interface

FDA UDI

Class I (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
FS DISPOSABLE INTERFACE FDA UDI
Generic Name
Laser beam delivery unit holder FDA UDI
Device Name
20 PROCEDURE PACK FDA UDI
Model / Reference
590106AN FDA UDI
Description
20 PROCEDURE PACK FDA UDI

Identifiers

Catalog Number
590106AN FDA UDI
Primary DI / UDI-DI
15050474534688 FDA UDI
FDA Product Code
HNO FDA UDI
GEX FDA UDI
GMDN Term
Laser beam delivery unit holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4370 FDA UDI
878.4810 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laser beam delivery unit holder

Fs Disposable Interface by Johnson & Johnson Surgical Vision, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser beam delivery unit holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Johnson & Johnson Surgical Vision, Inc.

Sources (1)

  • FDA UDI 555d9105-726e-4b32-a312-8b7f7beef6c4 35 fields · synced Jun 9, 2026