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Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
ADAPTOR, MDI, 22 OD X 22 ID FDA UDI
Model / Reference
HUD1659 FDA UDI
Description
ADAPTOR, MDI, 22 OD X 22 ID FDA UDI

Identifiers

Catalog Number
HUD1659 FDA UDI
Primary DI / UDI-DI
10197344012541 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Straight/elbow breathing circuit connector, single-use

Hudson Rci by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI d3d1fb5a-d202-4ea3-b1e3-70974c46c320 36 fields · synced May 30, 2026