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Suction Tubing

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Suction Tubing FDA UDI
Generic Name
Closed-suction breathing circuit connector/switch FDA UDI
Device Name
Standard CSS, Adult, 72-hours, Tracheostomy, 305mm, 14Fr, Standard Switch, sterile, latex-free FDA UDI
Model / Reference
VEN56061400 FDA UDI
Description
Standard CSS, Adult, 72-hours, Tracheostomy, 305mm, 14Fr, Standard Switch, sterile, latex-free FDA UDI

Identifiers

Primary DI / UDI-DI
00848530095925 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Closed-suction breathing circuit connector/switch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Closed-suction breathing circuit connector/switch

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

Similar devices

Also classified as Closed-suction breathing circuit connector/switch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SUNSET HEALTHCARE SOLUTIONS, Inc.

Sources (1)

  • FDA UDI 6b5083ac-3d21-4cc6-b45c-ae8796ab5fe2 34 fields · synced May 30, 2026