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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
Aerosol delivery tubing FDA UDI
Device Name
INLET TUBING,SINGLE PATIENT USE,25" FDA UDI
Model / Reference
IPN044602 FDA UDI
Description
INLET TUBING,SINGLE PATIENT USE,25" FDA UDI

Identifiers

Catalog Number
500-50 FDA UDI
Primary DI / UDI-DI
04026704597895 FDA UDI
510(k) Number
K001213 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Aerosol delivery tubing 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Aerosol delivery tubing

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

Similar devices

Also classified as Aerosol delivery tubing.

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 6f60d4ed-417e-4909-a8fa-b7f1aad08934 36 fields · synced May 30, 2026