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Zeos

FDA UDI

Class II (US FDA UDI)

by Santa Barbara Imaging Systems, Inc.

Identity

Trade Name
ZEOS FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
5MM LIGHT GUIDE, GREY FDA UDI
Model / Reference
84-20-5002 FDA UDI
Description
5MM LIGHT GUIDE, GREY FDA UDI

Identifiers

Catalog Number
84-20-5002 FDA UDI
Primary DI / UDI-DI
00812231030349 FDA UDI
FDA Product Code
FST FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fibreoptic light cable

Zeos by Santa Barbara Imaging Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Santa Barbara Imaging Systems, Inc.

Sources (1)

  • FDA UDI ff2c2799-dfba-4c1c-98de-51ba03727a4d 35 fields · synced Jun 6, 2026