Identity

Trade Name
MC Kit FDA UDI
Generic Name
Anaesthesia conduction filter FDA UDI
Device Name
This kit contains: 2 OF5001, 1 BF5000, 1 BF1438. FDA UDI
Model / Reference
OF5001SP FDA UDI
Description
This kit contains: 2 OF5001, 1 BF5000, 1 BF1438. FDA UDI

Identifiers

Catalog Number
OF5001SP FDA UDI
Primary DI / UDI-DI
00848530050443 FDA UDI
GMDN Term
Anaesthesia conduction filter FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

MC Kit by SUNSET HEALTHCARE SOLUTIONS, Inc. — 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

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

Manufacturer

Sources (1)

  • FDA UDI 2f5856fd-5f44-4b2e-85a9-a519938dc497 35 fields · synced May 30, 2026