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Hudson Rci

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Aerosol face mask, non-rebreathing FDA UDI
Device Name
AEROSOL MASK,INF, 22MM CONN FDA UDI
Model / Reference
RSH395826 FDA UDI
Description
AEROSOL MASK,INF, 22MM CONN FDA UDI

Identifiers

Catalog Number
RSH395826 FDA UDI
Primary DI / UDI-DI
10197344010554 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Aerosol face mask, non-rebreathing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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: Aerosol face mask, non-rebreathing

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

Similar devices

Also classified as Aerosol face mask, non-rebreathing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 27f3696e-1944-4a05-b513-75ddad24b6b3 36 fields · synced Jun 6, 2026