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Bacteria Filter

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Bacteria Filter FDA UDI
Generic Name
Anaesthesia conduction filter FDA UDI
Device Name
Suction Final Bacteria Filter 1/4" - 3/8" Barbed - 1/Pack FDA UDI
Model / Reference
BF1438S-1 FDA UDI
Description
Suction Final Bacteria Filter 1/4" - 3/8" Barbed - 1/Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00848530099510 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Anaesthesia conduction filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia conduction filter

Bacteria Filter by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class II — 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 c02f9787-6f59-4426-9d2a-a7ed5ff7a391 34 fields · synced May 30, 2026