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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
Non-rebreathing valve, single-use FDA UDI
Device Name
Pulmonary Function Filter FDA UDI
Model / Reference
IPN060009 FDA UDI
Description
Pulmonary Function Filter FDA UDI

Identifiers

Catalog Number
1603 FDA UDI
Primary DI / UDI-DI
14026704656247 FDA UDI
510(k) Number
K925217 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Category: Non-rebreathing valve, single-use

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

Similar devices

Also classified as Non-rebreathing valve, single-use.

Cleared under the same submission

K925217 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 1bdba70f-dcce-482d-94c9-8d94263f80d2 36 fields · synced Jun 7, 2026