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Quik Fil

FDA UDI

Class II (US FDA UDI)

by Southmedic Incorporated

Identity

Trade Name
Quik Fil FDA UDI
Generic Name
Sevoflurane anaesthesia vaporizer FDA UDI
Device Name
Quik Fil Adapter for use with sevoflurane FDA UDI
Model / Reference
M40000 FDA UDI
Description
Quik Fil Adapter for use with sevoflurane FDA UDI

Identifiers

Catalog Number
M40000 FDA UDI
Primary DI / UDI-DI
10620974002038 FDA UDI
510(k) Number
K945993 FDA UDI
FDA Product Code
CAD FDA UDI
GMDN Term
Sevoflurane anaesthesia vaporizer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5880 FDA UDI
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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sevoflurane anaesthesia vaporizer

Quik Fil by Southmedic Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sevoflurane anaesthesia vaporizer.

Cleared under the same submission

K945993 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Southmedic Incorporated

Sources (1)

  • FDA UDI e24d3acf-0d50-4a70-b7ad-c59d3929c937 36 fields · synced Jun 1, 2026