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Tracheostomy and Suction Accessory

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Tracheostomy and Suction Accessory FDA UDI
Generic Name
Closed-suction breathing circuit connector/switch FDA UDI
Device Name
Adult 72hr Closed Suction Catheter Endotracheal - 16FR 530mm FDA UDI
Model / Reference
VEN77253016M FDA UDI
Description
Adult 72hr Closed Suction Catheter Endotracheal - 16FR 530mm FDA UDI

Identifiers

Primary DI / UDI-DI
00848530106232 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

Category: Closed-suction breathing circuit connector/switch

Tracheostomy and Suction Accessory 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 d4c8f007-36e4-4920-840e-fe6040664f8b 34 fields · synced Jun 8, 2026