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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
Suction system catheter, general-purpose FDA UDI
Device Name
5fr Chimney Catheter, Gloves, Cup - KIT - Delee FDA UDI
Model / Reference
TRAKIT5-C FDA UDI
Description
5fr Chimney Catheter, Gloves, Cup - KIT - Delee FDA UDI

Identifiers

Primary DI / UDI-DI
00848530107062 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Suction system catheter, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction system catheter, general-purpose

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

Similar devices

Also classified as Suction system catheter, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3750cb9a-4e1a-4d05-b7f6-b559427a605b 34 fields · synced Jun 1, 2026