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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
Ventilator breathing circuit, single-use FDA UDI
Device Name
Pediatric ISO-GARD Drain Breathing Circuit Dual Heated Limb with Single Drain FDA UDI
Model / Reference
IPN913848 FDA UDI
Description
Pediatric ISO-GARD Drain Breathing Circuit Dual Heated Limb with Single Drain FDA UDI

Identifiers

Catalog Number
880-25KIT FDA UDI
Primary DI / UDI-DI
14026704660565 FDA UDI
FDA Product Code
OGG FDA UDI
GMDN Term
Ventilator breathing circuit, single-use 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

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: Ventilator breathing circuit, single-use

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

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 027a4d2f-e279-471f-a374-f0753225a9e5 35 fields · synced Jun 8, 2026