Porter/Brn Pedo W/Avs

FDA UDI

Class II (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name: PORTER/BRN PEDO W/AVS FDA UDI
Generic Name: Anaesthesia breathing circuit, reusable FDA UDI
Device Name: PORTER/BRN PEDO W/AVS FDA UDI
Model / Reference: 5155-4AV FDA UDI
Description: PORTER/BRN PEDO W/AVS FDA UDI

Identifiers

Catalog Number: 5155-4AV FDA UDI
Primary DI / UDI-DI: 00816711020929 FDA UDI
FDA Product Code: CBN FDA UDI
GMDN Term: Anaesthesia breathing circuit, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5430 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Anaesthesia breathing circuit, reusable

Porter/Brn Pedo W/Avs by Parker Hannifin Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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30MM UNIFLOW COAXIAL BREATHING SYSTEM WITH LUER ELBOW, AND LIMB, 2.4M — Intersurgical Incorporated · Class I
Ultipor™ Anesthesia Breathing Circuit System - Pediatric Machine Kit — Global Life Sciences Solutions USA LLC · Class II
Trulink — SPACELABS HEALTHCARE (WASHINGTON), INC · Class II
Respiration Tubing — VBM Medizintechnik GmbH · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Parker Hannifin Corp.

Sources (1)

FDA UDI 0b59e2cf-44e7-4b90-8d8d-23e522e62c31 34 fields · synced Jun 1, 2026