Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: HUDSON RCI FDA UDI
Generic Name: Therapeutic agent nebulizer, benchtop FDA UDI
Device Name: NEBULIZER,SMALL VOLUME,ISO, MICRO MIST FDA UDI
Model / Reference: IPN049830 FDA UDI
Description: NEBULIZER,SMALL VOLUME,ISO, MICRO MIST FDA UDI

Identifiers

Catalog Number: 41890 FDA UDI
Primary DI / UDI-DI: 14026704661500 FDA UDI
510(k) Number: K930525 FDA UDI
FDA Product Code: CAF FDA UDI
GMDN Term: Therapeutic agent nebulizer, benchtop FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5630 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Therapeutic agent nebulizer, benchtop

Hudson Rci by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic agent nebulizer, benchtop.

InnoSpire Essence — RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD · Class II
Sidestream — RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD · Class II
AirLife™ — Airlife, Inc. · Class II
AirLife™ — VYAIRE MEDICAL, INC. · Class II
Salter AIRE Elite — SALTER LABS · Class II
InnoSpire Elegance — RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD · Class II
InnoSpire Mini — RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD · Class II
Sidestream — RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD · Class II

Cleared under the same submission

K930525 also covers:

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI b7134ccf-6a8d-459d-84e5-0debe0c1a77d 36 fields · synced May 31, 2026