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Respiratory Accessory

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Respiratory Accessory FDA UDI
Generic Name
Anaesthesia conduction filter FDA UDI
Device Name
Ventilator Felt Filter 1/8" x 3" Dia FDA UDI
Model / Reference
VF006NS FDA UDI
Description
Ventilator Felt Filter 1/8" x 3" Dia FDA UDI

Identifiers

Primary DI / UDI-DI
00848530061326 FDA UDI
FDA Product Code
JRL FDA UDI
GMDN Term
Anaesthesia conduction filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia conduction filter

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

Similar devices

Also classified as Anaesthesia conduction filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7e869bc2-87df-4731-a8af-b5bb842a7ca2 34 fields · synced Jun 8, 2026