← Back to catalogue

Tracheostomy and Suction Accessory

FDA UDI

Class II (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
Neo/Pediatric, 72-Hr, Tracheostomy, Standard CSS, 305mm, MDI Port, 8Fr, Swivel Connectors, Sterile, Latex-Free FDA UDI
Model / Reference
VEN77230508M FDA UDI
Description
Neo/Pediatric, 72-Hr, Tracheostomy, Standard CSS, 305mm, MDI Port, 8Fr, Swivel Connectors, Sterile, Latex-Free FDA UDI

Identifiers

Primary DI / UDI-DI
00848530106195 FDA UDI
FDA Product Code
GYC FDA UDI
GMDN Term
Closed-suction breathing circuit connector/switch FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1310 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

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 II — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 89f330ec-9b9c-4e9b-8fd6-2b9e9a464e25 34 fields · synced May 30, 2026