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Newport Medical

FDA UDI

Class II (US FDA UDI)

by Newport Medical Instruments

Identity

Trade Name
Newport Medical FDA UDI
Generic Name
Microbial medical gas filter, single-use FDA UDI
Device Name
Filters FDA UDI
Model / Reference
FLT3209P-C FDA UDI
Description
Filters FDA UDI

Identifiers

Primary DI / UDI-DI
10884521541467 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Microbial medical gas filter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

No

FDA UDI

Dimensions & Sizes

Size
Width — 1.38 Inch FDA UDI
Length — 2 Inch FDA UDI

Category: Microbial medical gas filter, single-use

Newport Medical by Newport Medical Instruments — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microbial medical gas filter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ac69dc3-37ce-4c93-a0d8-309798c181e2 35 fields · synced May 30, 2026