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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
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
ADAPTOR,METERED DOSE INHALER FDA UDI
Model / Reference
IPN042692 FDA UDI
Description
ADAPTOR,METERED DOSE INHALER FDA UDI

Identifiers

Catalog Number
1659 FDA UDI
Primary DI / UDI-DI
04026704595099 FDA UDI
510(k) Number
K900783 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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: Straight/elbow breathing circuit connector, single-use

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

Similar devices

Also classified as Straight/elbow breathing circuit connector, single-use.

Cleared under the same submission

K900783 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 832e7bf9-f6bd-4bbc-b5bc-d20cb8e259a1 36 fields · synced Jun 8, 2026