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Exhalation Port Circuit

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Exhalation Port Circuit FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
Filtered Exhalation Port Circuit without Filters FDA UDI
Model / Reference
Filtered Exhalation Port Circuit without Filters FDA UDI
Description
Filtered Exhalation Port Circuit without Filters FDA UDI

Identifiers

Catalog Number
1069211 FDA UDI
Primary DI / UDI-DI
00606959042339 FDA UDI
FDA Product Code
MNT FDA UDI
GMDN Term
Ventilator breathing circuit, 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

Category: Ventilator breathing circuit, single-use

Exhalation Port Circuit by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 8044b6d5-2de5-4a15-b9b0-1c254d6b10e8 36 fields · synced May 30, 2026