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Ulti-MistHME/F

FDA UDI

Class II (US FDA UDI)

by King Systems Corporation.

Identity

Trade Name
Ulti-MistHME/F FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name
HME/F ULTI-MIST FDA UDI
Model / Reference
MS-111 FDA UDI
Description
HME/F ULTI-MIST FDA UDI

Identifiers

Catalog Number
MS-111 FDA UDI
Primary DI / UDI-DI
00612649205175 FDA UDI
510(k) Number
K983817 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Heat/moisture exchanger/microbial medical gas 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 55 Milliliter FDA UDI
Weight — 34 Gram FDA UDI

Category: Heat/moisture exchanger/microbial medical gas filter

Ulti-MistHME/F by King Systems Corporation. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger/microbial medical gas filter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04723842-bf88-4025-9590-d6490c6dceb1 37 fields · synced Jun 8, 2026