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Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Therapeutic agent vaporizer, benchtop FDA UDI
Device Name
AQUATHERM III,ELECTRONIC HEATER FDA UDI
Model / Reference
IPN924849 FDA UDI
Description
AQUATHERM III,ELECTRONIC HEATER FDA UDI

Identifiers

Catalog Number
050-14 FDA UDI
Primary DI / UDI-DI
14026704733634 FDA UDI
FDA Product Code
BZE FDA UDI
GMDN Term
Therapeutic agent vaporizer, benchtop FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5270 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Therapeutic agent vaporizer, 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 vaporizer, benchtop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 78c689d9-9d7f-4448-8c66-7966b4825d23 35 fields · synced Jun 6, 2026