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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
Heated respiratory humidifier FDA UDI
Device Name
RIGHT ANGLE ADULT TEMP,SINGLE 100K FDA UDI
Model / Reference
IPN913736 FDA UDI
Description
RIGHT ANGLE ADULT TEMP,SINGLE 100K FDA UDI

Identifiers

Catalog Number
380-92 FDA UDI
Primary DI / UDI-DI
14026704659422 FDA UDI
510(k) Number
K760866 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Heated respiratory humidifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5450 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
MRI Safety
MR Unsafe FDA UDI

Category: Heated respiratory humidifier

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

Similar devices

Also classified as Heated respiratory humidifier.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 725db45f-ee90-4970-ac0c-21329cc26f10 36 fields · synced Jun 1, 2026