← Back to catalogue

Hudson Rci

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
Breathing Circuit (10mm) FDA UDI
Model / Reference
IPN045187 FDA UDI
Description
Breathing Circuit (10mm) FDA UDI

Identifiers

Catalog Number
780-07 FDA UDI
Primary DI / UDI-DI
04026704398386 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Ventilator breathing circuit, 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ventilator breathing circuit, single-use

Hudson Rci by Teleflex Incorporated — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 652f3bac-aa65-4b43-9c9d-73cf5f4ae244 35 fields · synced May 29, 2026