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Suction Kit

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Suction Kit FDA UDI
Generic Name
Respirator filter/cartridge, particulates FDA UDI
Device Name
(1)RES025S (1) RES025 (1) BF516TS (1) RES023S FDA UDI
Model / Reference
AWAS003SUCTKIT FDA UDI
Description
(1)RES025S (1) RES025 (1) BF516TS (1) RES023S FDA UDI

Identifiers

Primary DI / UDI-DI
00848530090142 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Respirator filter/cartridge, particulates FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Respirator filter/cartridge, particulates

Suction Kit by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respirator filter/cartridge, particulates.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 52acdc87-80ff-43aa-afda-3a218409335b 34 fields · synced May 30, 2026