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Multiox, Intersurgical Ecolite, Adult, Adjustable Venturi Mask Kit, 1.8m

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
MULTIOX, INTERSURGICAL ECOLITE, ADULT, ADJUSTABLE VENTURI MASK KIT, 1.8M FDA UDI
Generic Name
Venturi oxygen face mask FDA UDI
Device Name
MULTIOX, INTERSURGICAL ECOLITE, ADULT, ADJUSTABLE VENTURI MASK KIT, 1.8M FDA UDI
Model / Reference
1117015 FDA UDI
Description
MULTIOX, INTERSURGICAL ECOLITE, ADULT, ADJUSTABLE VENTURI MASK KIT, 1.8M FDA UDI

Identifiers

Primary DI / UDI-DI
05030267151820 FDA UDI
FDA Product Code
BYF FDA UDI
GMDN Term
Venturi oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5600 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Venturi oxygen face mask

Multiox, Intersurgical Ecolite, Adult, Adjustable Venturi Mask Kit, 1.8m by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Venturi oxygen face mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c559e91e-44f4-45f4-bb9d-827b8eb69ce8 33 fields · synced May 31, 2026