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Intra.Ox Disposable Sheath

FDA UDI

Class II (US FDA UDI)

by Vioptix, Inc.

Identity

Trade Name
Intra.Ox Disposable Sheath FDA UDI
Generic Name
Tissue saturation oximeter sensor, single-use FDA UDI
Model / Reference
OXY2-STH-1 FDA UDI

Identifiers

Catalog Number
OXY-2-STH-1 FDA UDI
Primary DI / UDI-DI
B426OXY2STH10 FDA UDI
FDA Product Code
MUD FDA UDI
GMDN Term
Tissue saturation oximeter sensor, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Tissue saturation oximeter sensor, single-use

Intra.Ox Disposable Sheath by Vioptix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue saturation oximeter sensor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vioptix, Inc.

Sources (1)

  • FDA UDI e3a5997d-6909-4d00-abf6-4f502eb43225 33 fields · synced May 30, 2026