← Back to catalogue

Hudson Rci

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Breathing circuit condensate trap, single-use FDA UDI
Device Name
ISO-GARD WAND FDA UDI
Model / Reference
IPN045246 FDA UDI
Description
ISO-GARD WAND FDA UDI

Identifiers

Catalog Number
800 FDA UDI
Primary DI / UDI-DI
14026704611956 FDA UDI
FDA Product Code
BYH FDA UDI
GMDN Term
Breathing circuit condensate trap, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5995 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing circuit condensate trap, 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 condensate trap, 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 05e71fed-868c-4925-9328-59db20224f2a 35 fields · synced Jun 8, 2026