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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
Breathing circuit catheter mount, single-use FDA UDI
Device Name
EXPANDI-FLEX WITH CAP MOUNTED FDA UDI
Model / Reference
IPN044040 FDA UDI
Description
EXPANDI-FLEX WITH CAP MOUNTED FDA UDI

Identifiers

Catalog Number
22562 FDA UDI
Primary DI / UDI-DI
04026704388868 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Breathing circuit catheter mount, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing circuit catheter mount, single-use

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

Similar devices

Also classified as Breathing circuit catheter mount, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e023ba64-da2b-430f-8b80-2b3a6978f371 35 fields · synced Jun 8, 2026