Reusable Airway Adapter 9355-0303

by Zoll Medical Corporation

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00847946024055 UDI-DI	Date5 Oct 2021Listed	StatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Reusable Airway Adapter
Generic Name: Physiologic-monitoring defibrillation system
Model / Reference: 9355-0303

Primary DI / UDI-DI: 00847946024055
FDA Product Code: MKJ, DXN, LDD, DRM, DRT, DRO, DQA, CCK
GMDN Term: Physiologic-monitoring defibrillation system

Device Class: Class III
Regulation Number: 870.5310, 870.1130, 870.5300, 870.5200, 870.2300, 870.5550, 870.2700, 868.1400
GUDID distribution status: Not in Commercial Distribution

Other devices from Zoll Medical Corporation

R Series

Class IIb
Onestep Cpr Adult Electrodes

Class I
731 Ventilator

Class IIb
Zenix 1116-111075-21-Usa-0

Class III
Radiotransparent Defibrillation Electrode 8900-004041-01

Class III
Pedi Padz 8900-0813-01

Class III

See all devices from Zoll Medical Corporation →

Properties

Lot / Batch Number

Other properties (13)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No