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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
Rigid optical arthroscope, single-use FDA UDI
Device Name
ZEOS Camera, Single Use, 4MM, 30 DEG, EXT Length FDA UDI
Model / Reference
84-10-6431 FDA UDI
Description
ZEOS Camera, Single Use, 4MM, 30 DEG, EXT Length FDA UDI

Identifiers

Catalog Number
84-10-6431 FDA UDI
Primary DI / UDI-DI
00812231033548 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid optical arthroscope, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
MRI Safety
MR Unsafe FDA UDI

Category: Rigid optical arthroscope, single-use

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

Similar devices

Also classified as Rigid optical arthroscope, single-use.

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 a7bae82f-4db5-442e-8a50-52315213d716 35 fields · synced Jun 7, 2026