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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
Secretion suction kit FDA UDI
Device Name
Suction Kit (1 Kit), This Kit Contains: 1 RES025 Suction Tubing 6ft, 1 BF516TS Bacteria Filter 5/16in Barbed with Threaded NPT, 1 RES024XL Suction Tube Connector 16in, 1 RES023S Suction Canister 800cc, 1 RES028 Rubber Suction Elbow Connector. FDA UDI
Model / Reference
APRO030SKIT FDA UDI
Description
Suction Kit (1 Kit), This Kit Contains: 1 RES025 Suction Tubing 6ft, 1 BF516TS Bacteria Filter 5/16in Barbed with Threaded NPT, 1 RES024XL Suction Tube Connector 16in, 1 RES023S Suction Canister 800cc, 1 RES028 Rubber Suction Elbow Connector. FDA UDI

Identifiers

Catalog Number
APRO030SKIT FDA UDI
Primary DI / UDI-DI
00848530088781 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Secretion suction kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Secretion suction kit

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

Similar devices

Also classified as Secretion suction kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5d41c131-63fa-48a9-a93a-c263991681b0 35 fields · synced May 30, 2026