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Hudson Rci

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Cardiac sizing catheter FDA UDI
Device Name
In-Line NebTee with Valve 22mm O.D. x 18mm I.D. x 22mm O.D. FDA UDI
Model / Reference
IPN029719 FDA UDI
Description
In-Line NebTee with Valve 22mm O.D. x 18mm I.D. x 22mm O.D. FDA UDI

Identifiers

Catalog Number
1744 FDA UDI
Primary DI / UDI-DI
14026704658784 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Cardiac sizing catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5810 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiac sizing catheter

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

Similar devices

Also classified as Cardiac sizing catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 2bbd393a-31b3-4336-8226-9e9a42f2dddb 35 fields · synced May 30, 2026